22-20891490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891490
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891490
    reference: chr 22
allele count: 1
allele frequency: 8.300546175938376e-6
allele num: 120474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.77G>A
  hgvsp: ENSP00000392738.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.77G>A
  hgvsp: ENSP00000407742.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.35G>A
  hgvsp: ENSP00000416425.2:p.Arg12Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.155G>A
  hgvsp: ENSP00000409578.1:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.77G>A
  hgvsp: ENSP00000408742.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.77G>A
  hgvsp: ENSP00000443137.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.155G>A
  hgvsp: ENSP00000292733.7:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.155G>A
  hgvsp: ENSP00000263205.7:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.155G>A
  hgvsp: ENSP00000391108.1:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.167G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.77G>A
  hgvsp: ENSP00000390498.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.340G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.77G>A
  hgvsp: ENSP00000408794.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.155G>A
  hgvsp: ENSP00000372434.2:p.Arg52Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.77G>A
  hgvsp: ENSP00000384344.1:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.252G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-136G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*73G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg52Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-20891497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891497
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891497
    reference: chr 22
allele count: 2
allele frequency: 1.714442463310931e-5
allele num: 116656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.162G>A
  hgvsp: ENST00000433831.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.259G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+6G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+6G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.156+6G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

22-20891497-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891497
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891497
    reference: chr 22
allele count: 1
allele frequency: 8.572212316554656e-6
allele num: 116656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.162G>T
  hgvsp: ENSP00000391108.1:p.Arg54Ser
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.259G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+6G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+6G>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg54Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-20891498-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891498
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891498
    reference: chr 22
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.163C>A
  hgvsp: ENSP00000391108.1:p.Pro55Thr
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.260C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+7C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+7C>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro55Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-20891498-C-CCCTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891498
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891502
    reference: chr 22
allele count: 11122
allele frequency: 9.203905991393578e-2
allele num: 120840
alternate allele: CCCTA
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+8_156+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+8_341+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+8_168+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+8_36+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.164_167dupCCTA
  hgvsp: ENSP00000391108.1:p.Ter56Tyr
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+8_156+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+8_*74+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.261_264dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+8_156+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+8_-135+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+8_156+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+8_78+11dupCCTA
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.75e1
  variant carriers: 1174
genotype quality: GenotypeQuality
hgvs: p.Ter56Tyr
num of homozygotes: 990
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

22-20891498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891498
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891498
    reference: chr 22
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.163C>T
  hgvsp: ENSP00000391108.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.260C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+7C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+7C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 8472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro55Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-20891499-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891499
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891499
    reference: chr 22
allele count: 1
allele frequency: 9.942729875914731e-6
allele num: 100576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.164C>A
  hgvsp: ENSP00000391108.1:p.Pro55His
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.261C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+8C>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+8C>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro55His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-20891507-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891507
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891507
    reference: chr 22
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+5G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+5G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.264+5G>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

22-20891508-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891508
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891508
    reference: chr 22
allele count: 20
allele frequency: 1.663810458712543e-4
allele num: 120206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+6T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+6T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+17T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+17T>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.264+6T>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-20891515-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891515
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891515
    reference: chr 22
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+13A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+24A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+13A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

22-20891517-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891517
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891517
    reference: chr 22
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+15T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+15T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+26T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+26T>C
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

22-20891518-CTGGCAGAGAGACT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891518
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891505
    reference: chr 22
allele count: 1
allele frequency: 8.323761008173934e-6
allele num: 120138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18753
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: CTGGCAGAGAGACT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/22-20891535-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891535
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891535
    reference: chr 22
allele count: 92
allele frequency: 7.717343891554541e-4
allele num: 119212
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+33A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+33A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+44A>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+44A>C
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

22-20891535-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891535
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891535
    reference: chr 22
allele count: 2
allele frequency: 1.67768345468577e-5
allele num: 119212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+33A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+33A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+44A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+44A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-20891539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891539
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891539
    reference: chr 22
allele count: 144
allele frequency: 1.214513435554881e-3
allele num: 118566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+37G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+48G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+37G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+48G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11530
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 2
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-20891542-A-ACGTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891542
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891547
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 118132
alternate allele: ACGTTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+40_264+41insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+51_156+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+51_*74+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+51_341+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+51_36+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+40_167+41insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+51_156+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+51_-135+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+51_156+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+51_156+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+51_168+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+51_78+52insCGTTT
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-20891544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891544
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891544
    reference: chr 22
allele count: 57
allele frequency: 4.855444060173433e-4
allele num: 117394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+42C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+42C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15621
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

22-20891545-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20891545
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20891545
    reference: chr 22
allele count: 96507
allele frequency: 8.24902557439825e-1
allele num: 116992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.156+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.36+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*74+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.341+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.156+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-135+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.167+43A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.168+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.264+43A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.78+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.156+54A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.156+54A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 510
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 938
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 3.25e1
  variant carriers: 6162
genotype depth: GenotypeDepth
  all individuals: 10429
  bin: 2.75e1
  variant carriers: 10072
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.25e1
  variant carriers: 1647
genotype quality: GenotypeQuality
num of homozygotes: 39931
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-20905379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905379
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905379
    reference: chr 22
allele count: 1
allele frequency: 6.780580417683754e-5
allele num: 14748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3844C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-241C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3844C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13358C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3844C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-344C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-344C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

22-20905393-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905393
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905393
    reference: chr 22
allele count: 2
allele frequency: 1.338688085676038e-4
allele num: 14940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13344C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.-22C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3830C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3830C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-227C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3830C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-330C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

22-20905397-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905397
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905397
    reference: chr 22
allele count: 1
allele frequency: 6.682705159048383e-5
allele num: 14964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.-18C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3826C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13340C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3826C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-223C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3826C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-326C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-326C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

22-20905426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905426
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905426
    reference: chr 22
allele count: 1
allele frequency: 6.521455588887439e-5
allele num: 15334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3797G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3797G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3797G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13311G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.12G>A
  hgvsp: ENST00000457322.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-194G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-297G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-297G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly4Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

22-20905446-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905446
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905446
    reference: chr 22
allele count: 4
allele frequency: 2.556890820761954e-4
allele num: 15644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3777C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.32C>T
  hgvsp: ENSP00000415778.1:p.Ala11Val
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3777C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-174C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13291C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-277C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3777C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala11Val
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-20905480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905480
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905480
    reference: chr 22
allele count: 19
allele frequency: 1.133381054640897e-3
allele num: 16764
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-140G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13257G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3743G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3743G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+27G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3743G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-243G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-243G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

22-20905488-CGTTGGAGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905488
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905480
    reference: chr 22
allele count: 8
allele frequency: 4.663091629750524e-4
allele num: 17156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31079
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: CGTTGGAGG
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

22-20905500-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905500
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905500
    reference: chr 22
allele count: 60
allele frequency: 3.289834411667946e-3
allele num: 18238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3723T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+47T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-120T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13237T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3723T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3723T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-223T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-223T>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-20905535-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905535
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905535
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 39566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3688G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3688G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13202G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-85G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-85G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+82G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-188G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3688G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-188G>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

22-20905539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905539
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905539
    reference: chr 22
allele count: 12
allele frequency: 3.039667663002179e-4
allele num: 39478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-81G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3684G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-81G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+86G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3684G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13198G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-184G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3684G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-184G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

22-20905544-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905544
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905544
    reference: chr 22
allele count: 1
allele frequency: 2.370454653202484e-5
allele num: 42186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-76G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3679G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-76G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3679G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+91G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13193G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3679G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-179G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-179G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

22-20905556-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905556
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905556
    reference: chr 22
allele count: 2
allele frequency: 4.281188457915918e-5
allele num: 46716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3667C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-64C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3667C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-64C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-167C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+103C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3667C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13181C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-167C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

22-20905557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905557
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905557
    reference: chr 22
allele count: 1
allele frequency: 2.071079446607572e-5
allele num: 48284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-63G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+104G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3666G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3666G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-63G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-166G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13180G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3666G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

22-20905563-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905563
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905563
    reference: chr 22
allele count: 4
allele frequency: 7.581501137225171e-5
allele num: 52760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3660C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3660C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-57C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-57C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3660C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+110C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-160C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13174C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-160C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

22-20905567-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905567
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905567
    reference: chr 22
allele count: 331
allele frequency: 5.932537548840377e-3
allele num: 55794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-53C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13170C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-53C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3656C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3656C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-156C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+114C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3656C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-156C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 5
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

22-20905567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905567
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905567
    reference: chr 22
allele count: 2
allele frequency: 3.58461483313618e-5
allele num: 55794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+114C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13170C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3656C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-53C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3656C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-156C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3656C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-53C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-20905568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905568
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905568
    reference: chr 22
allele count: 7
allele frequency: 1.209273399440279e-4
allele num: 57886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13169G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3655G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3655G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3655G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-155G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+115G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-155G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-20905570-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905570
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905570
    reference: chr 22
allele count: 1
allele frequency: 1.641443156823479e-5
allele num: 60922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-50G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3653G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3653G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3653G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-50G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+117G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13167G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-153G>C
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-20905571-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905571
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905572
    reference: chr 22
allele count: 1
allele frequency: 1.606683804627249e-5
allele num: 62240
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13164dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-47dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3650dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-47dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+120dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-150dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3650dupG
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3650dupG
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-20905572-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905572
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905572
    reference: chr 22
allele count: 1
allele frequency: 1.583932587829062e-5
allele num: 63134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-48G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-48G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3651G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3651G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+119G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3651G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-151G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13165G>C
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

22-20905575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905575
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905575
    reference: chr 22
allele count: 116
allele frequency: 1.71061169114611e-3
allele num: 67812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13162G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3648G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+122G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-45G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-45G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3648G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3648G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-148G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-20905580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905580
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905580
    reference: chr 22
allele count: 1
allele frequency: 1.345062276383397e-5
allele num: 74346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.4C>T
  hgvsp: ENST00000423862.1:c.4C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3643C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3643C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+127C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13157C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3643C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-143C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe2Phe
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

22-20905582-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905582
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905582
    reference: chr 22
allele count: 1
allele frequency: 1.291689271228913e-5
allele num: 77418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.6A>G
  hgvsp: ENSP00000408875.1:p.Gln3Arg
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3641A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-38A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3641A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13155A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.39+129A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3641A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-141A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln3Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

22-20905591-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905591
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905591
    reference: chr 22
allele count: 1
allele frequency: 1.112025443142139e-5
allele num: 89926
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.15C>G
  hgvsp: ENSP00000408875.1:p.Pro6Arg
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-29C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3632C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-29C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3632C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13146C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-132C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro6Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

22-20905591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905591
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905591
    reference: chr 22
allele count: 1
allele frequency: 1.112025443142139e-5
allele num: 89926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3632C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3632C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.15C>T
  hgvsp: ENSP00000408875.1:p.Pro6Leu
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3632C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13146C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-132C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro6Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

22-20905592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905592
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905592
    reference: chr 22
allele count: 3
allele frequency: 3.211716341212744e-5
allele num: 93408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3631G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.16G>A
  hgvsp: ENST00000423862.1:c.16G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-131G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3631G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13145G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3631G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro6Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

22-20905593-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905593
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905593
    reference: chr 22
allele count: 14
allele frequency: 1.464404510365892e-4
allele num: 95602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-27A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13144A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3630A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3630A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.17A>G
  hgvsp: ENSP00000408875.1:p.Ser7Gly
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-27A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3630A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-130A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-130A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser7Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

22-20905599-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905599
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905599
    reference: chr 22
allele count: 4
allele frequency: 3.861152940267964e-5
allele num: 103596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.23C>G
  hgvsp: ENSP00000408875.1:p.Arg9Gly
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3624C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-21C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3624C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-124C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13138C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg9Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

22-20905600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905600
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905600
    reference: chr 22
allele count: 101
allele frequency: 9.592007293724358e-4
allele num: 105296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13137G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.24G>A
  hgvsp: ENSP00000408875.1:p.Arg9His
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3623G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3623G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-123G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg9His
num of homozygotes: 3
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-20905606-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905606
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905606
    reference: chr 22
allele count: 1
allele frequency: 9.057150620414817e-6
allele num: 110410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3617A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3617A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.30A>G
  hgvsp: ENSP00000408875.1:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3617A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13131A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-117A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn11Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-20905609-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905609
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905609
    reference: chr 22
allele count: 1
allele frequency: 8.948866178655165e-6
allele num: 111746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3614T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.-11T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.33T>G
  hgvsp: ENSP00000408875.1:p.Leu12Arg
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.-11T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3614T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13128T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3614T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-114T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.-11T>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-114T>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu12Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

22-20905620-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905620
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905620
    reference: chr 22
allele count: 1187
allele frequency: 1.019776972112923e-2
allele num: 116398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.44A>G
  hgvsp: ENSP00000408875.1:p.Met16Val
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3603A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13117A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3603A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.1A>G
  hgvsp: ENSP00000396461.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.1A>G
  hgvsp: ENSP00000413603.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.1A>G
  hgvsp: ENSP00000416109.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-103A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3603A>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-103A>G
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 68
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

22-20905621-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905621
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905621
    reference: chr 22
allele count: 1
allele frequency: 8.572065353426254e-6
allele num: 116658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13116T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.2T>C
  hgvsp: ENSP00000396461.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.2T>C
  hgvsp: ENSP00000413603.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3602T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3602T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3602T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.2T>C
  hgvsp: ENSP00000416109.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.45T>C
  hgvsp: ENSP00000408875.1:p.Met16Thr
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-102T>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-102T>C
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

22-20905622-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905622
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905622
    reference: chr 22
allele count: 868
allele frequency: 7.423498623060739e-3
allele num: 116926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3601G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.46G>C
  hgvsp: ENSP00000408875.1:p.Met16Ile
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.3G>C
  hgvsp: ENSP00000413603.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3601G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.3G>C
  hgvsp: ENSP00000396461.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3601G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.3G>C
  hgvsp: ENSP00000416109.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-101G>C
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13115G>C
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 19
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-20905622-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905622
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905622
    reference: chr 22
allele count: 1
allele frequency: 8.552417768503155e-6
allele num: 116926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.46G>T
  hgvsp: ENSP00000408875.1:p.Met16Ile
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.3G>T
  hgvsp: ENSP00000396461.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3601G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13115G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.3G>T
  hgvsp: ENSP00000413603.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.3G>T
  hgvsp: ENSP00000416109.1:p.Met1?
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3601G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-101G>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-101G>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

22-20905624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905624
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905624
    reference: chr 22
allele count: 1
allele frequency: 8.517887563884156e-6
allele num: 117400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3599G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.5G>A
  hgvsp: ENSP00000396461.1:p.Gly2Asp
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.48G>A
  hgvsp: ENSP00000408875.1:p.Gly17Asp
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.5G>A
  hgvsp: ENSP00000413603.1:p.Gly2Asp
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3599G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.5G>A
  hgvsp: ENSP00000416109.1:p.Gly2Asp
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-99G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13113G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly17Asp
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

22-20905628-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905628
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905628
    reference: chr 22
allele count: 1
allele frequency: 8.453799983092399e-6
allele num: 118290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3595C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3595C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.9C>T
  hgvsp: ENST00000424287.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3595C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.52C>T
  hgvsp: ENST00000423862.1:c.52C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.9C>T
  hgvsp: ENST00000428629.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.9C>T
  hgvsp: ENST00000420849.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-95C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-95C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe18Phe
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

22-20905633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905633
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905633
    reference: chr 22
allele count: 5
allele frequency: 4.187674835424379e-5
allele num: 119398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.14C>T
  hgvsp: ENSP00000413603.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.57C>T
  hgvsp: ENSP00000408875.1:p.Ser20Leu
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3590C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.14C>T
  hgvsp: ENSP00000396461.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3590C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.14C>T
  hgvsp: ENSP00000416109.1:p.Ser5Leu
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3590C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-90C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-90C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser20Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

22-20905634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905634
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905634
    reference: chr 22
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.15G>A
  hgvsp: ENST00000424287.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.58G>A
  hgvsp: ENST00000423862.1:c.58G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3589G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.15G>A
  hgvsp: ENST00000420849.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.15G>A
  hgvsp: ENST00000428629.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3589G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-89G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.58G>A
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

22-20905639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905639
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905639
    reference: chr 22
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3584C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.15+5C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.15+5C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13098C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.58+5C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3584C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-84C>T
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.15+5C>T
  variant of: http://identifiers.org/hgnc/14248
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.58+5C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

22-20905645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905645
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905645
    reference: chr 22
allele count: 5
allele frequency: 4.141609926610672e-5
allele num: 120726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3578G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13092G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.15+11G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.58+11G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000473028
  gene symbol: MED15
  hgvsc: ENST00000473028.1:n.169-3578G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416425
  ensembl transcript: ENST00000425759
  gene symbol: MED15
  hgvsc: ENST00000425759.2:c.37-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.15+11G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.15+11G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-78G>A
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3578G>A
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

22-20905646-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20905646
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20905646
    reference: chr 22
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000444604
  ensembl transcript: ENST00000542773
  gene symbol: MED15
  hgvsc: ENST00000542773.1:c.-134-13091C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000409578
  ensembl transcript: ENST00000444094
  gene symbol: MED15
  hgvsc: ENST00000444094.1:c.157-3577C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408742
  ensembl transcript: ENST00000451058
  gene symbol: MED15
  hgvsc: ENST00000451058.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408875
  ensembl transcript: ENST00000423862
  gene symbol: MED15
  hgvsc: ENST00000423862.1:c.58+12C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000396461
  ensembl transcript: ENST00000424287
  gene symbol: MED15
  hgvsc: ENST00000424287.1:c.15+12C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000292733
  ensembl transcript: ENST00000292733
  gene symbol: MED15
  hgvsc: ENST00000292733.7:c.157-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000415778
  ensembl transcript: ENST00000457322
  gene symbol: MED15
  hgvsc: ENST00000457322.1:c.40-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000407742
  ensembl transcript: ENST00000445987
  gene symbol: MED15
  hgvsc: ENST00000445987.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000372434
  ensembl transcript: ENST00000382974
  gene symbol: MED15
  hgvsc: ENST00000382974.2:c.157-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000384344
  ensembl transcript: ENST00000406969
  gene symbol: MED15
  hgvsc: ENST00000406969.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000391108
  ensembl transcript: ENST00000433831
  gene symbol: MED15
  hgvsc: ENST00000433831.1:c.*-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000408794
  ensembl transcript: ENST00000432052
  gene symbol: MED15
  hgvsc: ENST00000432052.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413636
  ensembl transcript: ENST00000441501
  gene symbol: MED15
  hgvsc: ENST00000441501.1:c.*75-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000263205
  ensembl transcript: ENST00000263205
  gene symbol: MED15
  hgvsc: ENST00000263205.7:c.157-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000486656
  gene symbol: MED15
  hgvsc: ENST00000486656.1:n.265-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000390498
  ensembl transcript: ENST00000445189
  gene symbol: MED15
  hgvsc: ENST00000445189.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000443137
  ensembl transcript: ENST00000541476
  gene symbol: MED15
  hgvsc: ENST00000541476.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000392738
  ensembl transcript: ENST00000414658
  gene symbol: MED15
  hgvsc: ENST00000414658.1:c.79-77C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000416109
  ensembl transcript: ENST00000420849
  gene symbol: MED15
  hgvsc: ENST00000420849.1:c.15+12C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl transcript: ENST00000477824
  gene symbol: MED15
  hgvsc: ENST00000477824.1:n.342-3577C>G
  variant of: http://identifiers.org/hgnc/14248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099917
  ensembl protein: ENSP00000413603
  ensembl transcript: ENST00000428629
  gene symbol: MED15
  hgvsc: ENST00000428629.1:c.15+12C>G
  variant of: http://identifiers.org/hgnc/14248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum

GenotypeDepth
all individuals: 426
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21805
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8906
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1930
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18251
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1165
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1281
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3756
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1090
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4975
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504664459825459e-5
allele num: 66460
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.798e0

MQ
type: SiteQuality
SIO_000300: 5.566e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.879139e6

QD
type: SiteQuality
SIO_000300: 1.136e1

GenotypeDepth
all individuals: 198
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8648
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1101
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4224
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17273
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 439
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2539
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19727
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4912
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 458
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053808098699078e-5
allele num: 65492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.816e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: 8.54e-1

DP
type: SiteQuality
SIO_000300: 1.937524e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

GenotypeDepth
all individuals: 548
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 439
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1685
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17273
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1101
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8648
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 647
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19727
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4224
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 7.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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Latino
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South Asian
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VQSLOD
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MQRankSum
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FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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Other
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ClippingRankSum
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QD
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VQSLOD
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DP
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 3.935972060535506e-1
allele num: 8590
num of homozygotes: 639

European (Finnish)
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African
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allele frequency: 1.263259402121504e-2
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Latino
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South Asian
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allele count: 2480
allele frequency: 1.511642082165062e-1
allele num: 16406
num of homozygotes: 206

European (Non-Finnish)
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allele count: 3950
allele frequency: 5.940206929740135e-2
allele num: 66496
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Other
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allele frequency: 7.888888888888888e-2
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FS
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: 9.1e-2

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
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
allele num: 11482
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.199e0

ReadPosRankSum
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SIO_000300: -1.141e0

BaseQRankSum
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SIO_000300: -1.403e0

VQSLOD
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DP
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SIO_000300: 1.813985e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.999e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

GenotypeDepth
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bin: 4.25e1
variant carriers: 6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

European (Finnish)
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allele count: 7
allele frequency: 1.074278698588091e-3
allele num: 6516
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 (Non-Finnish)
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allele count: 9
allele frequency: 1.36029745170944e-4
allele num: 66162
num of homozygotes: 0

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

African
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allele count: 4
allele frequency: 3.878975950349108e-4
allele num: 10312
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.0e-1

VQSLOD
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FS
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InbreedingCoeff
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SIO_000300: -1.5e-3

DP
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.416e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.106e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 498
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

DP
type: SiteQuality
SIO_000300: 1.756009e6

FS
type: SiteQuality
SIO_000300: 6.289e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

QD
type: SiteQuality
SIO_000300: 1.377e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.78e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 406
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11442
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: 10340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66234
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.175126590095097e-5
allele num: 16194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
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SIO_000300: -1.839e0

DP
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SIO_000300: 1.751566e6

InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQ
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SIO_000300: 5.403e1

FS
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QD
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SIO_000300: 1.122e1

ClippingRankSum
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SIO_000300: -2.296e0

BaseQRankSum
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SIO_000300: 2.96e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 894
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

European (Finnish)
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: 8522
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510437120502674e-5
allele num: 66206
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.899e1

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 4.6e-2

DP
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SIO_000300: 1.747018e6

VQSLOD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

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

South Asian
type: Population
allele count: 91
allele frequency: 5.691768826619965e-3
allele num: 15988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65798
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Other
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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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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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MQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 1.061195613724797e-3
allele num: 11308
num of homozygotes: 1

European (Non-Finnish)
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allele frequency: 1.876544716687517e-3
allele num: 65546
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African
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allele count: 7
allele frequency: 6.857366771159875e-4
allele num: 10208
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.537515375153752e-4
allele num: 6504
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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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

DP
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MQ
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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MQ
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SIO_000300: 5.462e1

InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 47
allele frequency: 7.236781326024698e-4
allele num: 64946
num of homozygotes: 0

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

African
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allele frequency: 3.941663381947182e-4
allele num: 10148
num of homozygotes: 0

Other
type: Population
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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: 5
allele frequency: 7.720815318097591e-4
allele num: 6476
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.222792858889704e-4
allele num: 8178
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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FS
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ReadPosRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1798

European (Finnish)
type: Population
allele count: 4998
allele frequency: 7.789900249376559e-1
allele num: 6416
num of homozygotes: 1939

African
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allele count: 9601
allele frequency: 9.436799685472774e-1
allele num: 10174
num of homozygotes: 4528

Latino
type: Population
allele count: 10014
allele frequency: 8.968296614723267e-1
allele num: 11166
num of homozygotes: 4486

Other
type: Population
allele count: 730
allele frequency: 8.371559633027523e-1
allele num: 872
num of homozygotes: 302

East Asian
type: Population
allele count: 6807
allele frequency: 8.385070214338507e-1
allele num: 8118
num of homozygotes: 2858

South Asian
type: Population
allele count: 12323
allele frequency: 7.860058680954203e-1
allele num: 15678
num of homozygotes: 4882

European (Non-Finnish)
type: Population
allele count: 52034
allele frequency: 8.05879073225127e-1
allele num: 64568
num of homozygotes: 20936

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

GenotypeQuality
all individuals: 1033
bin: 6.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.973684210526316e-3
allele num: 6080
num of homozygotes: 1

South Asian
type: Population
allele count: 4
allele frequency: 5.030181086519115e-4
allele num: 7952
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 2.392344497607655e-3
allele num: 418
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 1.075268817204301e-2
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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SIO_000300: 1.729e0

ClippingRankSum
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SIO_000300: 1.6e-1

BaseQRankSum
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SIO_000300: -7.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.65e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.3314e5

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1038
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.517766497461929e-4
allele num: 6304
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
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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: 8026
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 4.545454545454545e-3
allele num: 440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -1.589e0

ClippingRankSum
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SIO_000300: -2.76e-1

VQSLOD
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SIO_000300: 1.81e0

QD
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SIO_000300: 5.84e0

ReadPosRankSum
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SIO_000300: 7.29e-1

InbreedingCoeff
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SIO_000300: -7.679999999999999e-2

MQ
type: SiteQuality
SIO_000300: 4.996e1

DP
type: SiteQuality
SIO_000300: 3.48152e5

GenotypeDepth
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variant carriers: 15

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 6

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 8

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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variant carriers: 58

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2515
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variant carriers: 3

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 60
allele frequency: 8.625646923519264e-3
allele num: 6956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1454
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.183e1

DP
type: SiteQuality
SIO_000300: 3.89938e5

InbreedingCoeff
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SIO_000300: -7.04e-2

MQRankSum
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SIO_000300: 1.35e-1

BaseQRankSum
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SIO_000300: -1.231e0

FS
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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: 0

GenotypeQuality
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GenotypeQuality
all individuals: 544
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3492
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: 11110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19492
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.71e-2

BaseQRankSum
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MQ
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QD
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DP
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MQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 9.370000000000001e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 1499
bin: 3.75e1
variant carriers: 3

Latino
type: Population
allele count: 1
allele frequency: 6.067961165048543e-4
allele num: 1648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 3.100134339154697e-4
allele num: 19354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.767012687427913e-4
allele num: 1734
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 4
allele frequency: 1.166861143523921e-3
allele num: 3428
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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FS
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SIO_000300: 2.2969e1

InbreedingCoeff
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SIO_000300: -3.02e-2

BaseQRankSum
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SIO_000300: -1.724e0

DP
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SIO_000300: 7.7643e5

ReadPosRankSum
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 614
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 666
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13376
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 584
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22959
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 508
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2515
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 882
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 731
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5376
bin: 9.75e1
variant carriers: 108

GenotypeQuality
all individuals: 351
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 6.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.420816257789255e-5
allele num: 35626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.275830678197542e-4
allele num: 13182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.557632398753894e-4
allele num: 6420
num of homozygotes: 0

East Asian
type: Population
allele count: 109
allele frequency: 2.752525252525253e-2
allele num: 3960
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4302
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.52e0

QD
type: SiteQuality
SIO_000300: 1.338e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

DP
type: SiteQuality
SIO_000300: 1.073189e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000407742
ensembl transcript: ENST00000445987
gene symbol: MED15
hgvsc: ENST00000445987.1:c.79-143C>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 3685
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1252
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2596
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5638
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1372
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1861
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20190
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1647
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18087
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1289
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2173
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20435
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.422475106685633e-4
allele num: 7030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

MQ
type: SiteQuality
SIO_000300: 5.929e1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.626e0

QD
type: SiteQuality
SIO_000300: 1.496e1

DP
type: SiteQuality
SIO_000300: 1.134584e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000443137
ensembl transcript: ENST00000541476
gene symbol: MED15
hgvsc: ENST00000541476.1:c.79-141A>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 19574
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1258
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1764
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4040
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18921
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2371
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 717
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1290
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1741
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1373
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5321
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1142
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 517
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19318
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5298
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.848428835489834e-4
allele num: 5410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13834
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.164324e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

FS
type: SiteQuality
SIO_000300: 6.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.633e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

QD
type: SiteQuality
SIO_000300: 1.338e1

MQRankSum
type: SiteQuality
SIO_000300: -2.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000473028
gene symbol: MED15
hgvsc: ENST00000473028.1:n.169-3632C>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5465
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25505
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13661
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1293
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2241
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 717
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1309
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1511
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3852
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1522
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1392
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14071
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.391207568169171e-4
allele num: 7188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.003e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -3.626e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 9.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.286375e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000392738
ensembl transcript: ENST00000414658
gene symbol: MED15
hgvsc: ENST00000414658.1:c.79-132C>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2241
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1309
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3852
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 717
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13661
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1392
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5465
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1293
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25505
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1511
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14071
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1404
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48316
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.754385964912281e-4
allele num: 5700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7188
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.286375e6

VQSLOD
type: SiteQuality
SIO_000300: -3.626e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.003e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.15e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408742
ensembl transcript: ENST00000451058
gene symbol: MED15
hgvsc: ENST00000451058.1:c.79-131G>A
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1352
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27272
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5817
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 717
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2420
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3403
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1328
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12136
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1343
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1397
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5362
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 12560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 1

East Asian
type: Population
allele count: 2
allele frequency: 3.333333333333333e-4
allele num: 6000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.990287397500199e-5
allele num: 50244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.321161e6

QD
type: SiteQuality
SIO_000300: 1.282e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000292733
ensembl transcript: ENST00000292733
gene symbol: MED15
hgvsc: ENST00000292733.7:c.157-130A>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2491
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11364
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1296
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3075
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1339
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 28392
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 717
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1242
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1232
bin: 1.75e1
variant carriers: 7

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5945
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1402
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11746
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5386
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1238
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.942577411709857e-4
allele num: 51478
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.146788990825688e-4
allele num: 8720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.70004933399112e-4
allele num: 8108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15054
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 1.339651e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.425e1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000409578
ensembl transcript: ENST00000444094
gene symbol: MED15
hgvsc: ENST00000444094.1:c.157-3624C>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1417
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 706
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1413
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7907
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1947
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6925
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3084
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32376
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5425
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5058
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30895
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.155635062611807e-5
allele num: 55900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

DP
type: SiteQuality
SIO_000300: 1.425495e6

FS
type: SiteQuality
SIO_000300: 4.755e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.213e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408794
ensembl transcript: ENST00000432052
gene symbol: MED15
hgvsc: ENST00000432052.1:c.79-123G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000477824
gene symbol: MED15
hgvsc: ENST00000477824.1:n.342-3623G>A
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 616
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3255
bin: 3.25e1
variant carriers: 7

GenotypeDepth
all individuals: 7216
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 1030
bin: 5.25e1
variant carriers: 8

GenotypeDepth
all individuals: 1444
bin: 3.75e1
variant carriers: 6

GenotypeDepth
all individuals: 438
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7148
bin: 2.75e1
variant carriers: 6

GenotypeDepth
all individuals: 33017
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 1303
bin: 4.75e1
variant carriers: 5

GenotypeDepth
all individuals: 279
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 710
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 674
bin: 1.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1696
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1423
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 32
bin: 8.75e1
variant carriers: 3

GenotypeDepth
all individuals: 79
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 147
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 9.75e1
variant carriers: 37

GenotypeDepth
all individuals: 53
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7423
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1696
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 692
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5506
bin: 9.75e1
variant carriers: 96

GenotypeQuality
all individuals: 5267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31532
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1535
bin: 8.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7034
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.543558438255119e-4
allele num: 15726
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.219512195121951e-3
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 93
allele frequency: 1.637208647278361e-3
allele num: 56804
num of homozygotes: 3

African
type: Population
allele count: 1
allele frequency: 1.067235859124867e-4
allele num: 9370
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.058460271716756e-4
allele num: 9716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.446608e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.277e1

FS
type: SiteQuality
SIO_000300: 1.288e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000443137
ensembl transcript: ENST00000541476
gene symbol: MED15
hgvsc: ENST00000541476.1:c.79-117A>G
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000413636
ensembl transcript: ENST00000441501
gene symbol: MED15
hgvsc: ENST00000441501.1:c.*75-117A>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1314
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 332
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5018
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1467
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7788
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3818
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1573
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35092
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 440
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 279
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 244
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 429
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5517
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.326963906581741e-4
allele num: 7536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e0

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.500157e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000390498
ensembl transcript: ENST00000445189
gene symbol: MED15
hgvsc: ENST00000445189.1:c.79-114T>G
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000415778
ensembl transcript: ENST00000457322
gene symbol: MED15
hgvsc: ENST00000457322.1:c.40-114T>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 147
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 874
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 441
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35438
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4391
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4058
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1325
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1628
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8021
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1478
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 333
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4518
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34227
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5528
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 377
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.218132073125233e-5
allele num: 16082
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 1.517661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408794
ensembl transcript: ENST00000432052
gene symbol: MED15
hgvsc: ENST00000432052.1:c.79-103A>G
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000416425
ensembl transcript: ENST00000425759
gene symbol: MED15
hgvsc: ENST00000425759.2:c.37-103A>G
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000292733
ensembl transcript: ENST00000292733
gene symbol: MED15
hgvsc: ENST00000292733.7:c.157-103A>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1749
bin: 4.25e1
variant carriers: 135

GenotypeDepth
all individuals: 1997
bin: 3.75e1
variant carriers: 131

GenotypeDepth
all individuals: 38
bin: 9.25e1
variant carriers: 14

GenotypeDepth
all individuals: 165
bin: 9.75e1
variant carriers: 109

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 17

GenotypeDepth
all individuals: 289
bin: 1.75e1
variant carriers: 28

GenotypeDepth
all individuals: 2298
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 1475
bin: 4.75e1
variant carriers: 113

GenotypeDepth
all individuals: 1140
bin: 5.25e1
variant carriers: 115

GenotypeDepth
all individuals: 8635
bin: 2.75e1
variant carriers: 71

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

GenotypeDepth
all individuals: 35438
bin: 2.25e1
variant carriers: 40

GenotypeDepth
all individuals: 4993
bin: 3.25e1
variant carriers: 88

GenotypeDepth
all individuals: 445
bin: 1.25e1
variant carriers: 14

GenotypeDepth
all individuals: 47
bin: 8.75e1
variant carriers: 18

GenotypeDepth
all individuals: 314
bin: 6.75e1
variant carriers: 43

GenotypeDepth
all individuals: 184
bin: 7.25e1
variant carriers: 41

GenotypeDepth
all individuals: 103
bin: 7.75e1
variant carriers: 27

GenotypeDepth
all individuals: 480
bin: 6.25e1
variant carriers: 46

GenotypeDepth
all individuals: 769
bin: 5.75e1
variant carriers: 70

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

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 2168
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 228
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6333
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2401
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6611
bin: 9.75e1
variant carriers: 1102

GenotypeQuality
all individuals: 2092
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 34685
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1190
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 944
bin: 8.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

Latino
type: Population
allele count: 64
allele frequency: 5.745062836624776e-3
allele num: 11140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.208062582802347e-4
allele num: 63404
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.393665158371041e-3
allele num: 884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

African
type: Population
allele count: 1106
allele frequency: 1.095483359746434e-1
allele num: 10096
num of homozygotes: 68

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 1.608646e6

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 1.613e1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000384344
ensembl transcript: ENST00000406969
gene symbol: MED15
hgvsc: ENST00000406969.1:c.79-102T>C
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000486656
gene symbol: MED15
hgvsc: ENST00000486656.1:n.265-102T>C
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000443137
ensembl transcript: ENST00000541476
gene symbol: MED15
hgvsc: ENST00000541476.1:c.79-102T>C
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1758
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5034
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2020
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8643
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1495
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 35505
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2187
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1136
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6387
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6378
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572970082109038e-5
allele num: 63574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

QD
type: SiteQuality
SIO_000300: 1.515e1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 1.610963e6

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408794
ensembl transcript: ENST00000432052
gene symbol: MED15
hgvsc: ENST00000432052.1:c.79-101G>C
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000413636
ensembl transcript: ENST00000441501
gene symbol: MED15
hgvsc: ENST00000441501.1:c.*75-101G>C
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000392738
ensembl transcript: ENST00000414658
gene symbol: MED15
hgvsc: ENST00000414658.1:c.79-101G>C
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 180
bin: 9.75e1
variant carriers: 28

GenotypeDepth
all individuals: 5174
bin: 3.25e1
variant carriers: 124

GenotypeDepth
all individuals: 1208
bin: 5.25e1
variant carriers: 74

GenotypeDepth
all individuals: 291
bin: 1.75e1
variant carriers: 27

GenotypeDepth
all individuals: 8628
bin: 2.75e1
variant carriers: 79

GenotypeDepth
all individuals: 1890
bin: 4.25e1
variant carriers: 118

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 6

GenotypeDepth
all individuals: 809
bin: 5.75e1
variant carriers: 41

GenotypeDepth
all individuals: 42
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 17

GenotypeDepth
all individuals: 34945
bin: 2.25e1
variant carriers: 49

GenotypeDepth
all individuals: 2069
bin: 7.5e0
variant carriers: 6

GenotypeDepth
all individuals: 112
bin: 7.75e1
variant carriers: 10

GenotypeDepth
all individuals: 188
bin: 7.25e1
variant carriers: 10

GenotypeDepth
all individuals: 2166
bin: 3.75e1
variant carriers: 147

GenotypeDepth
all individuals: 73
bin: 8.25e1
variant carriers: 9

GenotypeDepth
all individuals: 333
bin: 6.75e1
variant carriers: 15

GenotypeDepth
all individuals: 491
bin: 6.25e1
variant carriers: 20

GenotypeDepth
all individuals: 1568
bin: 4.75e1
variant carriers: 76

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6301
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34232
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7207
bin: 9.75e1
variant carriers: 841

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1243
bin: 9.25e1
variant carriers: 4

Other
type: Population
allele count: 9
allele frequency: 1.01123595505618e-2
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 554
allele frequency: 6.795878312070658e-2
allele num: 8152
num of homozygotes: 16

European (Finnish)
type: Population
allele count: 182
allele frequency: 2.815594059405941e-2
allele num: 6464
num of homozygotes: 3

African
type: Population
allele count: 1
allele frequency: 9.873617693522907e-5
allele num: 10128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 102
allele frequency: 1.601004551875687e-3
allele num: 63710
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.931761343336905e-5
allele num: 11196
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.159526424996949e-3
allele num: 16386
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.6304e6

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.38e-2

QD
type: SiteQuality
SIO_000300: 1.577e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.48e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408742
ensembl transcript: ENST00000451058
gene symbol: MED15
hgvsc: ENST00000451058.1:c.79-101G>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000391108
ensembl transcript: ENST00000433831
gene symbol: MED15
hgvsc: ENST00000433831.1:c.*-101G>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000409578
ensembl transcript: ENST00000444094
gene symbol: MED15
hgvsc: ENST00000444094.1:c.157-3601G>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2069
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2166
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1568
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5174
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8628
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1208
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34945
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 809
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7207
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6301
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569612305760477e-5
allele num: 63710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.577e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.38e-2

DP
type: SiteQuality
SIO_000300: 1.6304e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.48e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.359e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000473028
gene symbol: MED15
hgvsc: ENST00000473028.1:n.169-3599G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000390498
ensembl transcript: ENST00000445189
gene symbol: MED15
hgvsc: ENST00000445189.1:c.79-99G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408794
ensembl transcript: ENST00000432052
gene symbol: MED15
hgvsc: ENST00000432052.1:c.79-99G>A
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 826
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1911
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 371
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2201
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8706
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1609
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1868
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5279
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1197
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 502
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34941
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6892
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 203
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

DP
type: SiteQuality
SIO_000300: 1.636623e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.843e0

MQRankSum
type: SiteQuality
SIO_000300: -2.292e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000408742
ensembl transcript: ENST00000451058
gene symbol: MED15
hgvsc: ENST00000451058.1:c.79-95C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000413636
ensembl transcript: ENST00000441501
gene symbol: MED15
hgvsc: ENST00000441501.1:c.*75-95C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000444604
ensembl transcript: ENST00000542773
gene symbol: MED15
hgvsc: ENST00000542773.1:c.-134-13109C>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1441
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5442
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1650
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1957
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35124
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2280
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1200
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8762
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6488
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6918
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34662
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64604
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.197891710589363e-4
allele num: 8348
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.99e0

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.259e1

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.649993e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000415778
ensembl transcript: ENST00000457322
gene symbol: MED15
hgvsc: ENST00000457322.1:c.40-90C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000384344
ensembl transcript: ENST00000406969
gene symbol: MED15
hgvsc: ENST00000406969.1:c.79-90C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000444604
ensembl transcript: ENST00000542773
gene symbol: MED15
hgvsc: ENST00000542773.1:c.-134-13104C>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 337
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 507
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35422
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5604
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2032
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1224
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8824
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2365
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6964
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
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: 8448
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.649704721397754e-5
allele num: 65362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.005e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.307e0

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.666599e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000473028
gene symbol: MED15
hgvsc: ENST00000473028.1:n.169-3589G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000392738
ensembl transcript: ENST00000414658
gene symbol: MED15
hgvsc: ENST00000414658.1:c.79-89G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000444604
ensembl transcript: ENST00000542773
gene symbol: MED15
hgvsc: ENST00000542773.1:c.-134-13103G>A
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1700
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8832
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5689
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2372
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35404
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1226
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2044
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6996
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2940
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6688
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65518
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: 6574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.669994e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-1

FS
type: SiteQuality
SIO_000300: 6.17e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.03e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000415778
ensembl transcript: ENST00000457322
gene symbol: MED15
hgvsc: ENST00000457322.1:c.40-84C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000443137
ensembl transcript: ENST00000541476
gene symbol: MED15
hgvsc: ENST00000541476.1:c.79-84C>T
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000473028
gene symbol: MED15
hgvsc: ENST00000473028.1:n.169-3584C>T
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1231
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8953
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2107
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 848
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5765
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2407
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35448
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1743
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65968
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.680293e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.491e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000391108
ensembl transcript: ENST00000433831
gene symbol: MED15
hgvsc: ENST00000433831.1:c.*-78G>A
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000415778
ensembl transcript: ENST00000457322
gene symbol: MED15
hgvsc: ENST00000457322.1:c.40-78G>A
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 1793
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 35422
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2420
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5893
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 858
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 511
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1242
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 339
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2125
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8998
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2487
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7094
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6847
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.809900069718801e-4
allele num: 8606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.769e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.219e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.451e0

DP
type: SiteQuality
SIO_000300: 1.688096e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl protein: ENSP00000416425
ensembl transcript: ENST00000425759
gene symbol: MED15
hgvsc: ENST00000425759.2:c.37-77C>G
variant of: http://identifiers.org/hgnc/14248

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000099917
ensembl transcript: ENST00000473028
gene symbol: MED15
hgvsc: ENST00000473028.1:n.169-3577C>G
variant of: http://identifiers.org/hgnc/14248

GenotypeDepth
all individuals: 147
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2338
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35323
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 395
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 288
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8965
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1227
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6802
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7339
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3007
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35223
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2