14-71060006-CACTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060006
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060002
    reference: chr 14
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.357+3_357+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.357+3_357+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.384+3_384+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.357+3_357+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.357+3_357+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.426+3_426+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.369+3_369+6delAAGT
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.378_381delAAGT
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39669
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: c.357+3_357+6delAAGT
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: CACTT
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-71060026-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060026
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060026
    reference: chr 14
allele count: 3
allele frequency: 2.473859550747106e-5
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.371T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.344T>C
  hgvsp: ENSP00000413343.2:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.344T>C
  hgvsp: ENSP00000451684.1:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.344T>C
  hgvsp: ENSP00000256379.5:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.344T>C
  hgvsp: ENSP00000394502.2:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.362T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.356T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.413T>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile115Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-71060031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060031
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060031
    reference: chr 14
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.339A>G
  hgvsp: ENST00000256379.5:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.351A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.339A>G
  hgvsp: ENST00000440435.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.366A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.357A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.408A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.339A>G
  hgvsp: ENST00000430055.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.339A>G
  hgvsp: ENST00000554963.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.611A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser113Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-71060033-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060033
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060033
    reference: chr 14
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.337T>A
  hgvsp: ENSP00000451684.1:p.Ser113Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.355T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.337T>A
  hgvsp: ENSP00000394502.2:p.Ser113Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.364T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.337T>A
  hgvsp: ENSP00000256379.5:p.Ser113Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.337T>A
  hgvsp: ENSP00000413343.2:p.Ser113Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.609T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.349T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.406T>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser113Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

14-71060035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060035
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060035
    reference: chr 14
allele count: 3
allele frequency: 2.473737157181259e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.347G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.335G>A
  hgvsp: ENSP00000394502.2:p.Gly112Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.335G>A
  hgvsp: ENSP00000451684.1:p.Gly112Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.353G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.335G>A
  hgvsp: ENSP00000256379.5:p.Gly112Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.404G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.335G>A
  hgvsp: ENSP00000413343.2:p.Gly112Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.607G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.362G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly112Glu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-71060046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060046
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060046
    reference: chr 14
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.324A>G
  hgvsp: ENST00000430055.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.324A>G
  hgvsp: ENST00000554963.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.351A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.336A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.342A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.324A>G
  hgvsp: ENST00000440435.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.393A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.324A>G
  hgvsp: ENST00000256379.5:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.596A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala108Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

14-71060072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060072
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060072
    reference: chr 14
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.325A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.298A>G
  hgvsp: ENSP00000394502.2:p.Ile100Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.316A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.310A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.298A>G
  hgvsp: ENSP00000413343.2:p.Ile100Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.298A>G
  hgvsp: ENSP00000451684.1:p.Ile100Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.367A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.298A>G
  hgvsp: ENSP00000256379.5:p.Ile100Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.570A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39545
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile100Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

14-71060074-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060074
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060074
    reference: chr 14
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.296A>G
  hgvsp: ENSP00000394502.2:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.296A>G
  hgvsp: ENSP00000413343.2:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.314A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.323A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.568A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.365A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.308A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.296A>G
  hgvsp: ENSP00000256379.5:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.296A>G
  hgvsp: ENSP00000451684.1:p.Tyr99Cys
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr99Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-71060081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060081
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060081
    reference: chr 14
allele count: 11
allele frequency: 9.093013259266607e-5
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.289G>A
  hgvsp: ENSP00000451684.1:p.Asp97Asn
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.561G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.289G>A
  hgvsp: ENSP00000256379.5:p.Asp97Asn
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.289G>A
  hgvsp: ENSP00000394502.2:p.Asp97Asn
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.316G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.289G>A
  hgvsp: ENSP00000413343.2:p.Asp97Asn
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.307G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.358G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.301G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp97Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-71060087-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060087
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060087
    reference: chr 14
allele count: 3
allele frequency: 2.482580559739164e-5
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.283C>G
  hgvsp: ENSP00000256379.5:p.Leu95Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.283C>G
  hgvsp: ENSP00000394502.2:p.Leu95Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.310C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.555C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.283C>G
  hgvsp: ENSP00000413343.2:p.Leu95Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.352C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.283C>G
  hgvsp: ENSP00000451684.1:p.Leu95Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.301C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.295C>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5233
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu95Val
num of homozygotes: 1
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-71060099-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060099
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060099
    reference: chr 14
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-4T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-4T>G
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
hgvs: n.547-4T>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-71060119-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060119
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060119
    reference: chr 14
allele count: 1
allele frequency: 8.368200836820084e-6
allele num: 119500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-24A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-24A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-24A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-71060129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060129
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060129
    reference: chr 14
allele count: 1407
allele frequency: 1.183088643358055e-2
allele num: 118926
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-34C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-34C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 1.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 2.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 21676
  bin: 2.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 7.25e1
  variant carriers: 3
num of homozygotes: 16
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

14-71060132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060132
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060132
    reference: chr 14
allele count: 23
allele frequency: 1.935603319138909e-4
allele num: 118826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-37T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-37T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-37T>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20343
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8041
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-71060140-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060140
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060140
    reference: chr 14
allele count: 3
allele frequency: 2.540908628925704e-5
allele num: 118068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-45T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-45T>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-45T>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19950
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2051
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4639
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

14-71060147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71060147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71060147
    reference: chr 14
allele count: 5
allele frequency: 4.271605782045586e-5
allele num: 117052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.302-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.287-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.275-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.275-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.275-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.547-52A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.344-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.275-52A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.293-52A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10380
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10936
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

14-71063280-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063280
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063280
    reference: chr 14
allele count: 5
allele frequency: 4.842708817604215e-5
allele num: 103248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.338A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.353A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+48A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+48A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+48A>C
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17238
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7294
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

14-71063281-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063281
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063281
    reference: chr 14
allele count: 1
allele frequency: 9.678855572117152e-6
allele num: 103318
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.352A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.337A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+47A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+47A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+47A>C
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3173
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

14-71063285-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063285
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063285
    reference: chr 14
allele count: 2
allele frequency: 1.933002145632382e-5
allele num: 103466
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.348C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+43C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.333C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+43C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+43C>G
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-71063305-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063305
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063305
    reference: chr 14
allele count: 1
allele frequency: 8.958646885974342e-6
allele num: 111624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+23A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.313A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.328A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+23A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+23A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

14-71063308-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063308
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063308
    reference: chr 14
allele count: 1
allele frequency: 8.813523470413002e-6
allele num: 113462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.325G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+20G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+20G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.310G>C
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-71063320-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063320
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063320
    reference: chr 14
allele count: 6
allele frequency: 5.093032731223686e-5
allele num: 117808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.313G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+8G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+8G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.298G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+8G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10183
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.546+8G>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

14-71063325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063325
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063325
    reference: chr 14
allele count: 1
allele frequency: 8.421619982819896e-6
allele num: 118742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.274+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.292+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.274+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.286+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.274+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.274+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.293A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.308A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.343+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.301+3A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.546+3A>G
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.546+3A>G
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-71063332-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063332
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063332
    reference: chr 14
allele count: 1
allele frequency: 8.360365180751095e-6
allele num: 119612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.339C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.288C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.270C>G
  hgvsp: ENST00000430055.2:c.270C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.270C>G
  hgvsp: ENST00000554963.1:c.270C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.297C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.542C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.301C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.270C>G
  hgvsp: ENST00000256379.5:c.270C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.270C>G
  hgvsp: ENST00000440435.2:c.270C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.286C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.282C>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala90Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

14-71063345-C-CGCTGTTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063345
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063352
    reference: chr 14
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: CGCTGTTG
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.250_256dupCAACAGC
  hgvsp: ENSP00000256379.5:p.Arg86ProfsTer14
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.522_528dupCAACAGC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.250_256dupCAACAGC
  hgvsp: ENSP00000451684.1:p.Arg86ProfsTer14
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.266_272dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.319_325dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.277_283dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.250_256dupCAACAGC
  hgvsp: ENSP00000413343.2:p.Arg86ProfsTer14
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.250_256dupCAACAGC
  hgvsp: ENSP00000394502.2:p.Arg86ProfsTer14
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.281_287dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.268_274dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.262_268dupCAACAGC
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg86ProfsTer14
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

14-71063346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063346
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063346
    reference: chr 14
allele count: 5
allele frequency: 4.161257032524385e-5
allele num: 120156
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.256C>T
  hgvsp: ENSP00000256379.5:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.256C>T
  hgvsp: ENSP00000451684.1:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.528C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.268C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.256C>T
  hgvsp: ENSP00000394502.2:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.283C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.272C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.325C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.256C>T
  hgvsp: ENSP00000413343.2:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.274C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.287C>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43352
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg86Trp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

14-71063357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063357
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063357
    reference: chr 14
allele count: 7
allele frequency: 5.814146649390345e-5
allele num: 120396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.272G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.263G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.245G>A
  hgvsp: ENSP00000394502.2:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.245G>A
  hgvsp: ENSP00000451684.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.245G>A
  hgvsp: ENSP00000413343.2:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.245G>A
  hgvsp: ENSP00000256379.5:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.276G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.517G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.261G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.314G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.257G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg82Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

14-71063358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063358
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063358
    reference: chr 14
allele count: 4
allele frequency: 3.321652189799206e-5
allele num: 120422
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.516C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.244C>T
  hgvsp: ENSP00000256379.5:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.271C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.262C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.244C>T
  hgvsp: ENSP00000413343.2:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.244C>T
  hgvsp: ENSP00000394502.2:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.275C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.313C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.244C>T
  hgvsp: ENSP00000451684.1:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.260C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.256C>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg82Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/14-71063359-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063359
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063359
    reference: chr 14
allele count: 3
allele frequency: 2.490990916186459e-5
allele num: 120434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.270T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.515T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.259T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.243T>G
  hgvsp: ENSP00000256379.5:p.Ile81Met
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.243T>G
  hgvsp: ENSP00000394502.2:p.Ile81Met
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.243T>G
  hgvsp: ENSP00000413343.2:p.Ile81Met
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.261T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.243T>G
  hgvsp: ENSP00000451684.1:p.Ile81Met
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.312T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.255T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.274T>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile81Met
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-71063364-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063364
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063364
    reference: chr 14
allele count: 3
allele frequency: 2.489957172736629e-5
allele num: 120484
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.238A>G
  hgvsp: ENSP00000256379.5:p.Ile80Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.510A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.238A>G
  hgvsp: ENSP00000394502.2:p.Ile80Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.250A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.238A>G
  hgvsp: ENSP00000413343.2:p.Ile80Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.307A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.238A>G
  hgvsp: ENSP00000451684.1:p.Ile80Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.254A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.265A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.269A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.256A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile80Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

14-71063369-AGAATGGGCTCTTGAGCAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063369
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063351
    reference: chr 14
allele count: 2
allele frequency: 1.659613310098747e-5
allele num: 120510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsp: ENSP00000394502.2:p.His72_Ile77del
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsp: ENSP00000413343.2:p.His72_Ile77del
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsp: ENSP00000256379.5:p.His72_Ile77del
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsp: ENSP00000451684.1:p.His72_Ile77del
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 43350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His72_Ile77del
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AGAATGGGCTCTTGAGCAT
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

14-71063376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063376
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063376
    reference: chr 14
allele count: 2
allele frequency: 1.659475605708596e-5
allele num: 120520
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.226C>T
  hgvsp: ENSP00000256379.5:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.226C>T
  hgvsp: ENSP00000413343.2:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.244C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.253C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.226C>T
  hgvsp: ENSP00000394502.2:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.226C>T
  hgvsp: ENSP00000451684.1:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.238C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.295C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.498C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.257C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.242C>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro76Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

14-71063377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063377
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063377
    reference: chr 14
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.225G>A
  hgvsp: ENST00000440435.2:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.225G>A
  hgvsp: ENST00000554963.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.225G>A
  hgvsp: ENST00000256379.5:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.225G>A
  hgvsp: ENST00000430055.2:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.241G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.237G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.252G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.294G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.243G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.256G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.497G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu75Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

14-71063382-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063382
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063382
    reference: chr 14
allele count: 1
allele frequency: 8.29737802854298e-6
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.220C>G
  hgvsp: ENSP00000451684.1:p.Gln74Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.220C>G
  hgvsp: ENSP00000413343.2:p.Gln74Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.289C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.220C>G
  hgvsp: ENSP00000394502.2:p.Gln74Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.251C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.232C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.247C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.492C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.220C>G
  hgvsp: ENSP00000256379.5:p.Gln74Glu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.236C>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.238C>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln74Glu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

14-71063403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063403
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063403
    reference: chr 14
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.199G>A
  hgvsp: ENSP00000394502.2:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.199G>A
  hgvsp: ENSP00000413343.2:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.217G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.215G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.268G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.230G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.199G>A
  hgvsp: ENSP00000451684.1:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.226G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.199G>A
  hgvsp: ENSP00000256379.5:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.211G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.471G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu67Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-71063404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063404
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063404
    reference: chr 14
allele count: 8
allele frequency: 6.646284726837697e-5
allele num: 120368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.198C>T
  hgvsp: ENST00000440435.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.229C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.210C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.216C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.214C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.198C>T
  hgvsp: ENST00000430055.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.267C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.470C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.198C>T
  hgvsp: ENST00000554963.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.198C>T
  hgvsp: ENST00000256379.5:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.225C>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile66Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

14-71063413-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063413
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063413
    reference: chr 14
allele count: 7
allele frequency: 5.823142833374927e-5
allele num: 120210
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.189G>A
  hgvsp: ENSP00000256379.5:p.Met63Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.189G>A
  hgvsp: ENSP00000394502.2:p.Met63Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.201G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.189G>A
  hgvsp: ENSP00000451684.1:p.Met63Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.216G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.220G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.258G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.205G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.207G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.461G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.189G>A
  hgvsp: ENSP00000413343.2:p.Met63Ile
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42498
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met63Ile
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-71063419-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063419
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063418
    reference: chr 14
allele count: 2
allele frequency: 1.666222340709144e-5
allele num: 120032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-5delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.251delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-1delG
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-1delG
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
hgvs: n.455-1delG
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: AC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

14-71063432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063432
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063432
    reference: chr 14
allele count: 1
allele frequency: 8.404067568703253e-6
allele num: 118990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.239G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-13G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-17G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-13G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-13G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/14-71063434-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063434
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063434
    reference: chr 14
allele count: 1
allele frequency: 8.405056481979558e-6
allele num: 118976
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-15G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-19G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.237G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-15G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-15G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

14-71063441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063441
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063441
    reference: chr 14
allele count: 1
allele frequency: 8.460093737838614e-6
allele num: 118202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-26G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-22G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.230G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-22G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-22G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

14-71063446-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063446
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063446
    reference: chr 14
allele count: 5
allele frequency: 4.251483767834975e-5
allele num: 117606
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-27C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.225C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-31C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-27C>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-27C>A
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10869
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

14-71063449-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063449
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063449
    reference: chr 14
allele count: 7
allele frequency: 5.983724269985639e-5
allele num: 116984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.222G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-30G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-30G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-34G>C
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

14-71063456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063456
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063456
    reference: chr 14
allele count: 1
allele frequency: 8.644387199391435e-6
allele num: 115682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-37G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.215G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-37G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-41G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-37G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9302
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

14-71063457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063457
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063457
    reference: chr 14
allele count: 1
allele frequency: 8.671372331385166e-6
allele num: 115322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.183-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.199-42C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.201-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.214-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.183-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.214C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.455-38C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.183-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.199-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.210-38C>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.183-38C>T
  variant of: http://identifiers.org/hgnc/19970
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19982
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6384
  bin: 3.25e1
  variant carriers: 0
hgvs: n.214C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-71063467-TAATTTTATAAGACATTCAAATTATTATATAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71063467
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71063434
    reference: chr 14
allele count: 2
allele frequency: 1.803914494452963e-5
allele num: 110870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7740
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: TAATTTTATAAGACATTCAAATTATTATATAAAA
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-71064284-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064284
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064284
    reference: chr 14
allele count: 1
allele frequency: 9.075068970524176e-6
allele num: 110192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+51G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+51G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+51G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-71064285-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064285
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064285
    reference: chr 14
allele count: 165
allele frequency: 1.496598639455782e-3
allele num: 110250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+50T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+50T>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+50T>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17331
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 3490
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 2
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

14-71064286-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064286
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064286
    reference: chr 14
allele count: 2
allele frequency: 1.81402604941407e-5
allele num: 110252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+49A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+49A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+49A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17360
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-71064289-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064289
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064289
    reference: chr 14
allele count: 4
allele frequency: 3.629698190595452e-5
allele num: 110202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+46G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+46G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+46G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

14-71064293-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064293
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064293
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 110316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+42T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+42T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+42T>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

14-71064295-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064295
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064295
    reference: chr 14
allele count: 2
allele frequency: 1.812809310588619e-5
allele num: 110326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+40A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+40A>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+40A>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-71064298-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064298
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064298
    reference: chr 14
allele count: 1
allele frequency: 9.061089867889309e-6
allele num: 110362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+37A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+37A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+37A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2053
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

14-71064314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064314
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064314
    reference: chr 14
allele count: 33487
allele frequency: 2.982401453483194e-1
allele num: 112282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+21G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+21G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 3.75e1
  variant carriers: 2665
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 5.75e1
  variant carriers: 2439
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 7.25e1
  variant carriers: 1115
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 2.25e1
  variant carriers: 639
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 397
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 599
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 3.25e1
  variant carriers: 2012
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 6.25e1
  variant carriers: 1944
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 8.75e1
  variant carriers: 421
genotype depth: GenotypeDepth
  all individuals: 14119
  bin: 2.75e1
  variant carriers: 1244
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.25e1
  variant carriers: 816
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.75e1
  variant carriers: 3166
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.25e1
  variant carriers: 2932
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.75e1
  variant carriers: 801
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 7.5e0
  variant carriers: 1176
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.5e0
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 6.75e1
  variant carriers: 1548
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 9.75e1
  variant carriers: 1355
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.25e1
  variant carriers: 3059
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.75e1
  variant carriers: 160
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.75e1
  variant carriers: 92
num of homozygotes: 6089
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-71064330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064330
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064330
    reference: chr 14
allele count: 2
allele frequency: 1.769034814605151e-5
allele num: 113056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+5G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+5G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+5G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.454+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-71064331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064331
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064331
    reference: chr 14
allele count: 2
allele frequency: 1.76728403789057e-5
allele num: 113168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454+4A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182+4A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209+4A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25011
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.454+4A>G
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-71064335-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064335
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064335
    reference: chr 14
allele count: 3
allele frequency: 2.643078658020863e-5
allele num: 113504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.213A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.182A>G
  hgvsp: ENSP00000394502.2:p.Asn61Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.198A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.200A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.209A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.182A>G
  hgvsp: ENSP00000413343.2:p.Asn61Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.211A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.198A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.182A>G
  hgvsp: ENSP00000256379.5:p.Asn61Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.182A>G
  hgvsp: ENSP00000451684.1:p.Asn61Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.454A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn61Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-71064356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064356
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064356
    reference: chr 14
allele count: 2
allele frequency: 1.725089704664643e-5
allele num: 115936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.188G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.192G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.190G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.177G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.179G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.161G>A
  hgvsp: ENSP00000451684.1:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.177G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.161G>A
  hgvsp: ENSP00000413343.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.161G>A
  hgvsp: ENSP00000394502.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.433G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.161G>A
  hgvsp: ENSP00000256379.5:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg54Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

14-71064358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064358
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064358
    reference: chr 14
allele count: 1
allele frequency: 8.597417335832316e-6
allele num: 116314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.177G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.159G>A
  hgvsp: ENST00000256379.5:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.175G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.190G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.175G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.431G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.159G>A
  hgvsp: ENST00000430055.2:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.159G>A
  hgvsp: ENST00000440435.2:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.186G>A
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.159G>A
  hgvsp: ENST00000554963.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.188G>A
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln53Gln
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

14-71064372-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064372
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064372
    reference: chr 14
allele count: 1
allele frequency: 8.442950980226608e-6
allele num: 118442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.174G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.161G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.145G>C
  hgvsp: ENSP00000256379.5:p.Val49Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.176G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.145G>C
  hgvsp: ENSP00000451684.1:p.Val49Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.163G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.161G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.145G>C
  hgvsp: ENSP00000413343.2:p.Val49Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.172G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.417G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.145G>C
  hgvsp: ENSP00000394502.2:p.Val49Leu
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val49Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

14-71064373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064373
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064373
    reference: chr 14
allele count: 10
allele frequency: 8.434263351438886e-5
allele num: 118564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.160A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.144A>G
  hgvsp: ENST00000440435.2:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.144A>G
  hgvsp: ENST00000430055.2:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.175A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.162A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.416A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.173A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.160A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.171A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.144A>G
  hgvsp: ENST00000554963.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.144A>G
  hgvsp: ENST00000256379.5:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu48Glu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-71064380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064380
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064380
    reference: chr 14
allele count: 1
allele frequency: 8.389824820457749e-6
allele num: 119192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.137A>G
  hgvsp: ENSP00000394502.2:p.Asn46Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.164A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.153A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.168A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.409A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.137A>G
  hgvsp: ENSP00000451684.1:p.Asn46Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.137A>G
  hgvsp: ENSP00000413343.2:p.Asn46Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.166A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.137A>G
  hgvsp: ENSP00000256379.5:p.Asn46Ser
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.153A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.155A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn46Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

14-71064392-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064392
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064392
    reference: chr 14
allele count: 1
allele frequency: 8.334305668994715e-6
allele num: 119986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.156A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.125A>G
  hgvsp: ENSP00000413343.2:p.Asp42Gly
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.141A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.125A>G
  hgvsp: ENSP00000394502.2:p.Asp42Gly
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.125A>G
  hgvsp: ENSP00000451684.1:p.Asp42Gly
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.154A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.143A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.141A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.125A>G
  hgvsp: ENSP00000256379.5:p.Asp42Gly
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.397A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.152A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp42Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-71064410-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064410
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064410
    reference: chr 14
allele count: 1
allele frequency: 8.307303781484682e-6
allele num: 120376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.125G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.107G>T
  hgvsp: ENSP00000451684.1:p.Arg36Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.123G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.134G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.107G>T
  hgvsp: ENSP00000413343.2:p.Arg36Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.379G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.107G>T
  hgvsp: ENSP00000394502.2:p.Arg36Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.136G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.123G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.107G>T
  hgvsp: ENSP00000256379.5:p.Arg36Ile
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.138G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg36Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

14-71064440-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064440
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064440
    reference: chr 14
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.95G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.106G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.349G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.108G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.77G>C
  hgvsp: ENSP00000413343.2:p.Ser26Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.93G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.77G>C
  hgvsp: ENSP00000256379.5:p.Ser26Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.93G>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.77G>C
  hgvsp: ENSP00000451684.1:p.Ser26Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.77G>C
  hgvsp: ENSP00000394502.2:p.Ser26Thr
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.104G>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser26Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

14-71064450-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064450
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064450
    reference: chr 14
allele count: 2
allele frequency: 1.661847309469206e-5
allele num: 120348
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.67A>G
  hgvsp: ENSP00000256379.5:p.Ile23Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.67A>G
  hgvsp: ENSP00000413343.2:p.Ile23Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.67A>G
  hgvsp: ENSP00000394502.2:p.Ile23Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.67A>G
  hgvsp: ENSP00000451684.1:p.Ile23Val
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.96A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.94A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.83A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.98A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.85A>G
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.339A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.83A>G
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile23Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/14-71064458-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064458
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064458
    reference: chr 14
allele count: 2
allele frequency: 1.663450662053363e-5
allele num: 120232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.90G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.59G>T
  hgvsp: ENSP00000394502.2:p.Trp20Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.86G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.77G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.88G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.59G>T
  hgvsp: ENSP00000451684.1:p.Trp20Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.59G>T
  hgvsp: ENSP00000413343.2:p.Trp20Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.75G>T
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.331G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.59G>T
  hgvsp: ENSP00000256379.5:p.Trp20Leu
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.75G>T
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Trp20Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-71064462-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71064462
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 71064462
    reference: chr 14
allele count: 1
allele frequency: 8.318775476249896e-6
allele num: 120210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556495
  gene symbol: MED6
  hgvsc: ENST00000556495.1:n.82T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000451684
  ensembl transcript: ENST00000554963
  gene symbol: MED6
  hgvsc: ENST00000554963.1:c.55T>C
  hgvsp: ENSP00000451684.1:p.Ser19Pro
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000413343
  ensembl transcript: ENST00000430055
  gene symbol: MED6
  hgvsc: ENST00000430055.2:c.55T>C
  hgvsp: ENSP00000413343.2:p.Ser19Pro
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553611
  gene symbol: MED6
  hgvsc: ENST00000553611.1:n.84T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000553523
  gene symbol: MED6
  hgvsc: ENST00000553523.1:n.86T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556044
  gene symbol: MED6
  hgvsc: ENST00000556044.1:n.71T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000394502
  ensembl transcript: ENST00000440435
  gene symbol: MED6
  hgvsc: ENST00000440435.2:c.55T>C
  hgvsp: ENSP00000394502.2:p.Ser19Pro
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000556423
  gene symbol: MED6
  hgvsc: ENST00000556423.1:n.71T>C
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259115
  ensembl transcript: ENST00000553982
  gene symbol: CTD-2540L5.5
  hgvsc: ENST00000553982.1:n.327T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133997
  ensembl protein: ENSP00000256379
  ensembl transcript: ENST00000256379
  gene symbol: MED6
  hgvsc: ENST00000256379.5:c.55T>C
  hgvsp: ENSP00000256379.5:p.Ser19Pro
  variant of: http://identifiers.org/hgnc/19970
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133997
  ensembl transcript: ENST00000554870
  gene symbol: MED6
  hgvsc: ENST00000554870.1:n.73T>C
  variant of: http://identifiers.org/hgnc/19970
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser19Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-71064483-C-A
type: Variant
location: Region
allele count: 1
allele frequency: 8.349615082744685e-6
allele num: 119766
alternate allele: A
canonical: true
consequence: stop gained
filter: PASS
hgvs: p.Gly12Ter
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 7163
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.25e1
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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.692e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 7.46e0

FS
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ClippingRankSum
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SIO_000300: 1.82e0

MQRankSum
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SIO_000300: -1.534e0

DP
type: SiteQuality
SIO_000300: 1.68065e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.258e0

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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bin: 9.75e1
variant carriers: 3

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.499235130027895e-5
allele num: 66678
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.361e1

MQRankSum
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SIO_000300: 3.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.681596e6

BaseQRankSum
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SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-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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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

MQRankSum
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SIO_000300: -1.033e0

VQSLOD
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SIO_000300: -6.560000000000001e-2

QD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.681539e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

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: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

DP
type: SiteQuality
SIO_000300: 1.681575e6

VQSLOD
type: SiteQuality
SIO_000300: -3.199e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 8.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.209e0

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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498965237995261e-5
allele num: 66682
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.072e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.681801e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.5e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
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: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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QD
type: SiteQuality
SIO_000300: 1.063e1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
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SIO_000300: -1.215e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.678874e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

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

FS
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.517e1

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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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

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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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.352813852813853e-4
allele num: 66528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.734003814808393e-4
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.167e1

FS
type: SiteQuality
SIO_000300: 1.329e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.743e0

VQSLOD
type: SiteQuality
SIO_000300: 2.98e0

DP
type: SiteQuality
SIO_000300: 1.678064e6

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

GenotypeQuality
all individuals: 11
bin: 7.5e0
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
all individuals: 451
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.485130111524163e-4
allele num: 8608
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.826e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.57e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 1.195e0

DP
type: SiteQuality
SIO_000300: 1.675247e6

MQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

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: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.406e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

MQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

DP
type: SiteQuality
SIO_000300: 1.663849e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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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variant carriers: 0

GenotypeQuality
all individuals: 5229
bin: 9.75e1
variant carriers: 1

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: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 1.520218911523259e-5
allele num: 65780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.623327e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.188e1

FS
type: SiteQuality
SIO_000300: 4.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e0

GenotypeQuality
all individuals: 27489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6425
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variant carriers: 1373

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 970
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GenotypeQuality
all individuals: 881
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variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1092
allele frequency: 1.668143350340656e-2
allele num: 65462
num of homozygotes: 14

East Asian
type: Population
allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 114
allele frequency: 1.732522796352584e-2
allele num: 6580
num of homozygotes: 1

Latino
type: Population
allele count: 40
allele frequency: 3.51000351000351e-3
allele num: 11396
num of homozygotes: 0

African
type: Population
allele count: 38
allele frequency: 3.827558420628526e-3
allele num: 9928
num of homozygotes: 0

Other
type: Population
allele count: 13
allele frequency: 1.45413870246085e-2
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 109
allele frequency: 6.739211079510326e-3
allele num: 16174
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 1.594441e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.487e0

GenotypeQuality
all individuals: 688
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variant carriers: 0

GenotypeQuality
all individuals: 477
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 109
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.754693805930865e-4
allele num: 11398
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: 6.19041723412158e-5
allele num: 16154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 2.019793981013937e-3
allele num: 9902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
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VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.567686e6

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.519e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-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
all individuals: 2510
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
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
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num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.613397305775973e-5
allele num: 65028
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 1.539349e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.323e0

FS
type: SiteQuality
SIO_000300: 3.209e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.14346787375833e-4
allele num: 15906
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

DP
type: SiteQuality
SIO_000300: 1.543592e6

QD
type: SiteQuality
SIO_000300: 1.61e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.037e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 6189
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.064142413111048e-5
allele num: 14156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56844
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.520287054926856e-4
allele num: 7246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.098e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 612
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5861
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7258
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3673
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.055171440666009e-5
allele num: 14174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56844
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.736e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

QD
type: SiteQuality
SIO_000300: 1.579e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.044072e6

MQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
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variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.51160585735857e-5
allele num: 56954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

DP
type: SiteQuality
SIO_000300: 1.073949e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
all individuals: 4691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7746
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.425070688030161e-5
allele num: 10610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.726e0

MQRankSum
type: SiteQuality
SIO_000300: -1.981e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 2.544e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.315152e6

FS
type: SiteQuality
SIO_000300: 6.284e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.302e0

GenotypeQuality
all individuals: 4316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 43585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3804
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.286775631500742e-5
allele num: 10768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 1.345239e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 47729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
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GenotypeQuality
all individuals: 4603
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.808073115003808e-4
allele num: 15756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.715e0

FS
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.400057e6

VQSLOD
type: SiteQuality
SIO_000300: 8.57e-1

GenotypeDepth
all individuals: 3487
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 1326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 431
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 198
bin: 2.75e1
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GenotypeQuality
all individuals: 1169
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.25312656328164e-5
allele num: 15992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65542
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

DP
type: SiteQuality
SIO_000300: 1.410421e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 3.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

VQSLOD
type: SiteQuality
SIO_000300: 9.08e-1

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4784
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variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49100
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
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GenotypeQuality
all individuals: 1171
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1369
bin: 7.75e1
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GenotypeQuality
all individuals: 834
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517496737382015e-5
allele num: 65898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 1.297e0

VQSLOD
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.420991e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4864
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 651
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 839
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variant carriers: 0

GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 49397
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51308821304282e-5
allele num: 66090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.986e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 4.733e1

DP
type: SiteQuality
SIO_000300: 1.428109e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 8.460000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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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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variant carriers: 0

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: 5

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.947533896639811e-4
allele num: 10178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51308821304282e-5
allele num: 66090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

QD
type: SiteQuality
SIO_000300: 1.085e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 1.428588e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
all individuals: 49592
bin: 6.25e1
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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variant carriers: 7

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 348
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.057210173382468e-4
allele num: 66212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

FS
type: SiteQuality
SIO_000300: 1.325e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 1.431313e6

GenotypeQuality
all individuals: 4875
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variant carriers: 0

GenotypeQuality
all individuals: 56
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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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GenotypeQuality
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variant carriers: 4

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: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020144362900547e-5
allele num: 66222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.108735491753207e-5
allele num: 16370
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.431646e6

FS
type: SiteQuality
SIO_000300: 1.015e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.851e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.681e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.875e1

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49605
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variant carriers: 1

GenotypeQuality
all individuals: 845
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 347
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1171
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variant carriers: 2

GenotypeQuality
all individuals: 431
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GenotypeQuality
all individuals: 1169
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 4881
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019961948479449e-5
allele num: 66226
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.778994719342852e-5
allele num: 10226
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: 16370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

DP
type: SiteQuality
SIO_000300: 1.431661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.119e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

QD
type: SiteQuality
SIO_000300: 1.247e1

GenotypeQuality
all individuals: 1173
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variant carriers: 3

GenotypeQuality
all individuals: 37
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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: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 55
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GenotypeQuality
all individuals: 4892
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.528028496392671e-5
allele num: 66254
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
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: 898
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

FS
type: SiteQuality
SIO_000300: 6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 1.432241e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

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: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 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: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.320185614849188e-4
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.547e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.724e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.579e0

FS
type: SiteQuality
SIO_000300: 4.278e0

DP
type: SiteQuality
SIO_000300: 1.432719e6

VQSLOD
type: SiteQuality
SIO_000300: -1.154e0

QD
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49608
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.775171065493646e-5
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
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: 16386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.43303e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.23e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

FS
type: SiteQuality
SIO_000300: 4.593e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.805e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

GenotypeQuality
all individuals: 428
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

VQSLOD
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SIO_000300: 7.18e-1

DP
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SIO_000300: 1.433123e6

MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.135e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
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allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66282
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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South Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66240
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 6.49e-1

QD
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e-1

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

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

East Asian
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allele count: 8
allele frequency: 9.300162752848175e-4
allele num: 8602
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66232
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.969e1

ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: -8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

VQSLOD
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BaseQRankSum
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SIO_000300: -1.411e0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.058137074099828e-4
allele num: 66154
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.026909222992402e-5
allele num: 66074
num of homozygotes: 0

Other
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ReadPosRankSum
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SIO_000300: 1.66e-1

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

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

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

European (Non-Finnish)
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allele count: 0
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African
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South Asian
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Latino
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Other
type: Population
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InbreedingCoeff
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SIO_000300: 2.3e-3

ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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DP
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MQ
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SIO_000300: 5.797e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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Other
type: Population
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 9.924573243350536e-5
allele num: 10076
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 8.3e-1

DP
type: SiteQuality
SIO_000300: 1.396966e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.256e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.82e-1

QD
type: SiteQuality
SIO_000300: 1.59e1

GenotypeQuality
all individuals: 1091
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534495457893445e-5
allele num: 65168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.342e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

DP
type: SiteQuality
SIO_000300: 1.372174e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-1

QD
type: SiteQuality
SIO_000300: 4.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.334e0

GenotypeQuality
all individuals: 808
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.457917261055635e-4
allele num: 11216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.573e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 1.338915e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

GenotypeQuality
all individuals: 276
bin: 7.5e0
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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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3398
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 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: 15910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.748334108166744e-5
allele num: 64530
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.795977011494253e-4
allele num: 11136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.093e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.508e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 1.290286e6

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeQuality
all individuals: 585
bin: 7.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564357674738752e-5
allele num: 63924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8034
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

DP
type: SiteQuality
SIO_000300: 1.222838e6

GenotypeQuality
all individuals: 102
bin: 2.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
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: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.34517766497462e-5
allele num: 15760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.227e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61092
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.612330198537095e-4
allele num: 7656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 6.18e-1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.16265e6

MQ
type: SiteQuality
SIO_000300: 4.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-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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GenotypeQuality
all individuals: 1861
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GenotypeQuality
all individuals: 18056
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568824323052305e-5
allele num: 63742
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

DP
type: SiteQuality
SIO_000300: 1.758737e6

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.815e0

VQSLOD
type: SiteQuality
SIO_000300: -1.972e-1

GenotypeQuality
all individuals: 11183
bin: 9.75e1
variant carriers: 160

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
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GenotypeQuality
all individuals: 7116
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 568
bin: 4.25e1
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GenotypeQuality
all individuals: 1291
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 152
allele frequency: 1.51605824855376e-2
allele num: 10026
num of homozygotes: 2

Other
type: Population
allele count: 2
allele frequency: 2.531645569620253e-3
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.869884575026233e-4
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568283043723731e-5
allele num: 63764
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.091464745688714e-4
allele num: 9162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

DP
type: SiteQuality
SIO_000300: 1.759677e6

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

FS
type: SiteQuality
SIO_000300: 1.613e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.421e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
all individuals: 1277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11100
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 392
bin: 2.5e0
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GenotypeQuality
all individuals: 913
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3498
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18771
bin: 6.25e1
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GenotypeQuality
all individuals: 1046
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 7.5e0
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GenotypeQuality
all individuals: 1072
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2018
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7117
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.972078181092939e-5
allele num: 10028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.091464745688714e-4
allele num: 9162
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.760245e6

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
all individuals: 822
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 7.5e0
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GenotypeQuality
all individuals: 806
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
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GenotypeQuality
all individuals: 1344
bin: 8.75e1
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
all individuals: 856
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GenotypeQuality
all individuals: 11094
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.366812227074236e-4
allele num: 9160
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.566e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.765575e6

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.12e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.634e0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
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variant carriers: 0

GenotypeQuality
all individuals: 198
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GenotypeQuality
all individuals: 2249
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21539
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variant carriers: 0

GenotypeQuality
all individuals: 329
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variant carriers: 0

GenotypeQuality
all individuals: 11107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 622
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9178
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 1.772751e6

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2245
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3480
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11113
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.364066193853428e-4
allele num: 8460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63798
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

FS
type: SiteQuality
SIO_000300: 2.11e0

DP
type: SiteQuality
SIO_000300: 1.776409e6

QD
type: SiteQuality
SIO_000300: 1.315e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.372e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

GenotypeQuality
all individuals: 2205
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
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variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3498
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 3.75e1
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GenotypeQuality
all individuals: 2804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.25e1
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GenotypeQuality
all individuals: 11115
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.087902523933855e-4
allele num: 9192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e-1

DP
type: SiteQuality
SIO_000300: 1.78148e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.886e0

QD
type: SiteQuality
SIO_000300: 1.055e1

GenotypeQuality
all individuals: 1498
bin: 7.75e1
variant carriers: 240

GenotypeQuality
all individuals: 17998
bin: 6.25e1
variant carriers: 119

GenotypeQuality
all individuals: 769
bin: 7.5e0
variant carriers: 57

GenotypeQuality
all individuals: 321
bin: 1.75e1
variant carriers: 164

GenotypeQuality
all individuals: 518
bin: 2.5e0
variant carriers: 16

GenotypeQuality
all individuals: 1711
bin: 2.25e1
variant carriers: 192

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 98

GenotypeQuality
all individuals: 259
bin: 3.25e1
variant carriers: 127

GenotypeQuality
all individuals: 4966
bin: 6.75e1
variant carriers: 128

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 78

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 82

GenotypeQuality
all individuals: 1063
bin: 8.25e1
variant carriers: 331

GenotypeQuality
all individuals: 27554
bin: 9.75e1
variant carriers: 25873

GenotypeQuality
all individuals: 1313
bin: 7.25e1
variant carriers: 121

GenotypeQuality
all individuals: 672
bin: 9.25e1
variant carriers: 314

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 102

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 160

GenotypeQuality
all individuals: 583
bin: 8.75e1
variant carriers: 308

European (Finnish)
type: Population
allele count: 1290
allele frequency: 1.951588502269289e-1
allele num: 6610
num of homozygotes: 131

South Asian
type: Population
allele count: 3325
allele frequency: 3.223773511731627e-1
allele num: 10314
num of homozygotes: 512

East Asian
type: Population
allele count: 4754
allele frequency: 5.566744730679157e-1
allele num: 8540
num of homozygotes: 1343

Other
type: Population
allele count: 232
allele frequency: 2.9e-1
allele num: 800
num of homozygotes: 34

Latino
type: Population
allele count: 2355
allele frequency: 2.052466445877636e-1
allele num: 11474
num of homozygotes: 259

European (Non-Finnish)
type: Population
allele count: 15135
allele frequency: 2.35278572316876e-1
allele num: 64328
num of homozygotes: 1780

African
type: Population
allele count: 6396
allele frequency: 6.260767423649177e-1
allele num: 10216
num of homozygotes: 2030

BaseQRankSum
type: SiteQuality
SIO_000300: -4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

QD
type: SiteQuality
SIO_000300: 1.717e1

DP
type: SiteQuality
SIO_000300: 2.315336e6

FS
type: SiteQuality
SIO_000300: 3.533e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.429999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeDepth
all individuals: 8641
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 464
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variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 507
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 9690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
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GenotypeQuality
all individuals: 772
bin: 9.25e1
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GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 7.25e1
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GenotypeQuality
all individuals: 151
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1438
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.09664633202242e-5
allele num: 64586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.701834e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.452e0

QD
type: SiteQuality
SIO_000300: 1.114e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
all individuals: 52
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 3331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
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GenotypeQuality
all individuals: 3271
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variant carriers: 2

GenotypeQuality
all individuals: 40
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.095496053242532e-5
allele num: 64610
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 10816
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.39e-1

VQSLOD
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DP
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MQRankSum
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SIO_000300: 5.5e-2

ReadPosRankSum
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SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 1.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.637358560563902e-5
allele num: 64692
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

DP
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MQRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
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SIO_000300: -8.0e-4

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.448e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12710
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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MQRankSum
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SIO_000300: 7.74e-1

FS
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SIO_000300: 6.29e-1

InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
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SIO_000300: -2.038e0

ReadPosRankSum
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SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.528397627926881e-5
allele num: 65428
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 2.1e-3

VQSLOD
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FS
type: SiteQuality
SIO_000300: 7.282e0

MQRankSum
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SIO_000300: 2.98e-1

QD
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ClippingRankSum
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SIO_000300: -1.128e0

MQ
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SIO_000300: 5.954e1

BaseQRankSum
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SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 1.731409e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516806212838248e-5
allele num: 65928
num of homozygotes: 0

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

East Asian
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South Asian
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MQRankSum
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SIO_000300: -3.1e-2

DP
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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SIO_000300: 3.82e-1

ReadPosRankSum
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ClippingRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
type: Population
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allele frequency: 1.156871818602499e-3
allele num: 8644
num of homozygotes: 0

Other
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allele num: 884
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
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QD
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FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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DP
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BaseQRankSum
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SIO_000300: 1.79e0

VQSLOD
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SIO_000300: 1.06e0

ReadPosRankSum
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SIO_000300: 4.04e-1

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

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

European (Non-Finnish)
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allele num: 66074
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European (Finnish)
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African
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South Asian
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East Asian
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Latino
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509206157561123e-5
allele num: 66260
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

QD
type: SiteQuality
SIO_000300: 1.639e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.0856e1

VQSLOD
type: SiteQuality
SIO_000300: -9.588e-1

DP
type: SiteQuality
SIO_000300: 1.766259e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.225874735400324e-5
allele num: 16062
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

QD
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SIO_000300: 1.145e1

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.552e0

DP
type: SiteQuality
SIO_000300: 1.770907e6

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 6.694e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.063e0

GenotypeQuality
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variant carriers: 0

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

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: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
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: 16262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508250128201261e-5
allele num: 66302
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-3

QD
type: SiteQuality
SIO_000300: 1.306e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.375e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.08e-1

FS
type: SiteQuality
SIO_000300: 9.04e-1

DP
type: SiteQuality
SIO_000300: 1.771921e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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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
all individuals: 9902
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variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738828029907842e-4
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
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: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

FS
type: SiteQuality
SIO_000300: 2.757e0

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

QD
type: SiteQuality
SIO_000300: 1.468e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.770789e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 30
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020509257860875e-5
allele num: 66214
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.362e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.769272e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

FS
type: SiteQuality
SIO_000300: 6.037e0

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510391493475109e-5
allele num: 66208
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.272e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

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