15-42092162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42092162
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42092162
    reference: chr 15
allele count: 3
allele frequency: 2.476759737793703e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-10919C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-10919C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.378+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.147+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.171+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.206+50C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12043
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9725
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

15-42092163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42092163
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42092163
    reference: chr 15
allele count: 2
allele frequency: 1.65144584083365e-5
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.147+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.378+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-10918G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-10918G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.171+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.206+51G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1713
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-42103032-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103032
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103032
    reference: chr 15
allele count: 1
allele frequency: 8.330695279828055e-6
allele num: 120038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.143G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.74G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-49G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

15-42103033-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103033
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103033
    reference: chr 15
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.144G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.75G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-48G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-48G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7460
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

15-42103070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103070
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103070
    reference: chr 15
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.181C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.112C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-11C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-11C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

15-42103071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103071
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103071
    reference: chr 15
allele count: 4
allele frequency: 3.304692663582287e-5
allele num: 121040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.113A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.182A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-10A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-10A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

15-42103072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103072
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103072
    reference: chr 15
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.183T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.114T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-9T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-9T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

15-42103076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103076
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103076
    reference: chr 15
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.148-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.118C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-130-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.115-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.172-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.379-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.187C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.207-5C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.207-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

15-42103101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103101
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103101
    reference: chr 15
allele count: 11
allele frequency: 9.065435965056865e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.227A>G
  hgvsp: ENSP00000397570.2:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.168A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.227A>G
  hgvsp: ENSP00000393099.2:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.227A>G
  hgvsp: ENSP00000426154.1:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.135A>G
  hgvsp: ENST00000505373.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.212A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.227A>G
  hgvsp: ENSP00000221214.6:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-110A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.143A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.227A>G
  hgvsp: ENSP00000427582.1:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.227A>G
  hgvsp: ENSP00000422132.1:p.Asn76Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.399A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.192A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn76Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-42103105-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103105
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103105
    reference: chr 15
allele count: 8
allele frequency: 6.592935669430205e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.139C>A
  hgvsp: ENSP00000421891.1:p.Pro47Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.216C>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.231C>A
  hgvsp: ENST00000456763.2:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.231C>A
  hgvsp: ENST00000514566.1:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.172C>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.147C>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.231C>A
  hgvsp: ENST00000221214.6:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.231C>A
  hgvsp: ENST00000457542.2:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.403C>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.231C>A
  hgvsp: ENST00000510535.1:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-106C>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.231C>A
  hgvsp: ENST00000512970.1:c.231C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.196C>A
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro47Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

15-42103106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103106
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103106
    reference: chr 15
allele count: 5
allele frequency: 4.120584793393878e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.232C>T
  hgvsp: ENSP00000426154.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.232C>T
  hgvsp: ENSP00000221214.6:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.173C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.232C>T
  hgvsp: ENSP00000427582.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.197C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.232C>T
  hgvsp: ENSP00000397570.2:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.148C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.232C>T
  hgvsp: ENSP00000393099.2:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.232C>T
  hgvsp: ENSP00000422132.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.404C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.217C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.140C>T
  hgvsp: ENSP00000421891.1:p.Pro47Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-105C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12122
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg78Trp
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: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

15-42103107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103107
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103107
    reference: chr 15
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.149G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.218G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.233G>A
  hgvsp: ENSP00000427582.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.233G>A
  hgvsp: ENSP00000393099.2:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.233G>A
  hgvsp: ENSP00000221214.6:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.198G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.233G>A
  hgvsp: ENSP00000426154.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.233G>A
  hgvsp: ENSP00000397570.2:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.405G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-104G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.174G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.233G>A
  hgvsp: ENSP00000422132.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.141G>A
  hgvsp: ENST00000505373.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg78Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

15-42103110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103110
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103110
    reference: chr 15
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.236A>G
  hgvsp: ENSP00000397570.2:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.144A>G
  hgvsp: ENST00000505373.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.221A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.236A>G
  hgvsp: ENSP00000427582.1:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-101A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.152A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.236A>G
  hgvsp: ENSP00000426154.1:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.236A>G
  hgvsp: ENSP00000393099.2:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.236A>G
  hgvsp: ENSP00000422132.1:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.236A>G
  hgvsp: ENSP00000221214.6:p.Lys79Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.201A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.177A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.408A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys79Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

15-42103115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103115
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103115
    reference: chr 15
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.241A>G
  hgvsp: ENSP00000427582.1:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.241A>G
  hgvsp: ENSP00000221214.6:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.206A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.149A>G
  hgvsp: ENSP00000421891.1:p.Gln50Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.241A>G
  hgvsp: ENSP00000397570.2:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.241A>G
  hgvsp: ENSP00000422132.1:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.226A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.182A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.241A>G
  hgvsp: ENSP00000426154.1:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.413A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.241A>G
  hgvsp: ENSP00000393099.2:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-96A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.157A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys81Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/15-42103116-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103116
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103116
    reference: chr 15
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.242A>C
  hgvsp: ENSP00000397570.2:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.242A>C
  hgvsp: ENSP00000393099.2:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-95A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.242A>C
  hgvsp: ENSP00000221214.6:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.158A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.242A>C
  hgvsp: ENSP00000422132.1:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.242A>C
  hgvsp: ENSP00000427582.1:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.414A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.183A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.227A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.242A>C
  hgvsp: ENSP00000426154.1:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.150A>C
  hgvsp: ENSP00000421891.1:p.Gln50His
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.207A>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys81Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-42103130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103130
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103130
    reference: chr 15
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.256C>T
  hgvsp: ENSP00000427582.1:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.241C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.256C>T
  hgvsp: ENSP00000422132.1:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.221C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.428C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.256C>T
  hgvsp: ENSP00000221214.6:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.256C>T
  hgvsp: ENSP00000397570.2:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.197C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.256C>T
  hgvsp: ENSP00000426154.1:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.164C>T
  hgvsp: ENSP00000421891.1:p.Pro55Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-81C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.172C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.256C>T
  hgvsp: ENSP00000393099.2:p.Leu86Phe
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu86Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

15-42103132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103132
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103132
    reference: chr 15
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.166C>T
  hgvsp: ENSP00000421891.1:p.Gln56Ter
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-79C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.174C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.258C>T
  hgvsp: ENST00000514566.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.199C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.258C>T
  hgvsp: ENST00000457542.2:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.258C>T
  hgvsp: ENST00000456763.2:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.243C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.430C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.258C>T
  hgvsp: ENST00000221214.6:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.258C>T
  hgvsp: ENST00000512970.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.258C>T
  hgvsp: ENST00000510535.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.223C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln56Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

15-42103134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103134
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103134
    reference: chr 15
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-77A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.260A>G
  hgvsp: ENSP00000393099.2:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.176A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.225A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.260A>G
  hgvsp: ENSP00000397570.2:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.260A>G
  hgvsp: ENSP00000427582.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.260A>G
  hgvsp: ENSP00000422132.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.260A>G
  hgvsp: ENSP00000221214.6:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.260A>G
  hgvsp: ENSP00000426154.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.168A>G
  hgvsp: ENST00000505373.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.201A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.245A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.432A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn87Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-42103136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103136
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103136
    reference: chr 15
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.262A>G
  hgvsp: ENSP00000422132.1:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.262A>G
  hgvsp: ENSP00000426154.1:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.227A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.170A>G
  hgvsp: ENSP00000421891.1:p.Gln57Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-75A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.262A>G
  hgvsp: ENSP00000393099.2:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.434A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.262A>G
  hgvsp: ENSP00000397570.2:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.262A>G
  hgvsp: ENSP00000221214.6:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.262A>G
  hgvsp: ENSP00000427582.1:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.203A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.247A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.178A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser88Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

15-42103137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103137
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103137
    reference: chr 15
allele count: 15
allele frequency: 1.236318079915601e-4
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.204G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.228G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.435G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.263G>A
  hgvsp: ENSP00000426154.1:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.263G>A
  hgvsp: ENSP00000427582.1:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.263G>A
  hgvsp: ENSP00000221214.6:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.171G>A
  hgvsp: ENST00000505373.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.263G>A
  hgvsp: ENSP00000422132.1:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.179G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.263G>A
  hgvsp: ENSP00000393099.2:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-74G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.263G>A
  hgvsp: ENSP00000397570.2:p.Ser88Asn
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.248G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser88Asn
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

15-42103141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103141
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103141
    reference: chr 15
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.439C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.232C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.267C>T
  hgvsp: ENST00000512970.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.267C>T
  hgvsp: ENST00000456763.2:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.267C>T
  hgvsp: ENST00000510535.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-70C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.208C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.175C>T
  hgvsp: ENSP00000421891.1:p.Gln59Ter
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.267C>T
  hgvsp: ENST00000457542.2:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.267C>T
  hgvsp: ENST00000221214.6:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.252C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.267C>T
  hgvsp: ENST00000514566.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.183C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln59Ter
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

15-42103147-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103147
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103147
    reference: chr 15
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+4A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+4A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.269+4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-42103157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103157
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103157
    reference: chr 15
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+14G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+14G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

15-42103160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103160
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103160
    reference: chr 15
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+17C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+17C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-42103164-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103164
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103164
    reference: chr 15
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+21A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+21A>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

15-42103174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103174
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103174
    reference: chr 15
allele count: 4
allele frequency: 3.300711303285858e-5
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+31T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+31T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7523
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-42103176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103176
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103176
    reference: chr 15
allele count: 7
allele frequency: 5.777293585553465e-5
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+33C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

15-42103187-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103187
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103188
    reference: chr 15
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+45dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+45dupT
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

15-42103188-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103188
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103188
    reference: chr 15
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.254+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.234+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.177+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.441+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.185+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-68+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.210+45T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.269+45T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

15-42103337-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103337
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103337
    reference: chr 15
allele count: 3
allele frequency: 2.474716644944154e-5
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-39G>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-39G>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

15-42103339-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103339
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103339
    reference: chr 15
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-37T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-37T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

15-42103347-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103347
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103347
    reference: chr 15
allele count: 6
allele frequency: 4.947963912849862e-5
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-29C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-29C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9511
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

15-42103350-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103350
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103350
    reference: chr 15
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-26C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-26C>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP

15-42103362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103362
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103362
    reference: chr 15
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-14C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-14C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

15-42103372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103372
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103372
    reference: chr 15
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270-4G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442-4G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.270-4G>A
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

15-42103376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103376
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103376
    reference: chr 15
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.178G>A
  hgvsp: ENSP00000421891.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.186G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-67G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.255G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.211G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.270G>A
  hgvsp: ENST00000456763.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.270G>A
  hgvsp: ENST00000457542.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.442G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.270G>A
  hgvsp: ENST00000221214.6:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.270G>A
  hgvsp: ENST00000512970.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.235G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.270G>A
  hgvsp: ENST00000510535.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.270G>A
  hgvsp: ENST00000514566.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu60Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

15-42103382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103382
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103382
    reference: chr 15
allele count: 11
allele frequency: 9.062896501721951e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-61C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.276C>T
  hgvsp: ENST00000510535.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.184C>T
  hgvsp: ENSP00000421891.1:p.His62Tyr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.276C>T
  hgvsp: ENST00000512970.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.276C>T
  hgvsp: ENST00000514566.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.192C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.241C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.276C>T
  hgvsp: ENST00000457542.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.448C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.276C>T
  hgvsp: ENST00000221214.6:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.217C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.276C>T
  hgvsp: ENST00000456763.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.261C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His62Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-42103383-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103383
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103383
    reference: chr 15
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.277A>C
  hgvsp: ENSP00000221214.6:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-60A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.218A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.277A>C
  hgvsp: ENSP00000397570.2:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.193A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.262A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.277A>C
  hgvsp: ENSP00000427582.1:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.277A>C
  hgvsp: ENSP00000422132.1:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.277A>C
  hgvsp: ENSP00000426154.1:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.277A>C
  hgvsp: ENSP00000393099.2:p.Ile93Leu
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.449A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.242A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.185A>C
  hgvsp: ENSP00000421891.1:p.His62Pro
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile93Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

15-42103385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103385
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103385
    reference: chr 15
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.279C>T
  hgvsp: ENST00000457542.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.195C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.279C>T
  hgvsp: ENST00000221214.6:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.279C>T
  hgvsp: ENST00000514566.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-58C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.279C>T
  hgvsp: ENST00000510535.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.279C>T
  hgvsp: ENST00000512970.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.451C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.279C>T
  hgvsp: ENST00000456763.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.220C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.187C>T
  hgvsp: ENSP00000421891.1:p.His63Tyr
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.264C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.244C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His63Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

15-42103391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103391
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103391
    reference: chr 15
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.285C>T
  hgvsp: ENST00000457542.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.270C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.285C>T
  hgvsp: ENST00000512970.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.285C>T
  hgvsp: ENST00000456763.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.285C>T
  hgvsp: ENST00000510535.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.193C>T
  hgvsp: ENSP00000421891.1:p.Pro65Ser
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.250C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.285C>T
  hgvsp: ENST00000221214.6:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.226C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.457C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.201C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.285C>T
  hgvsp: ENST00000514566.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro65Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-42103404-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103404
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103404
    reference: chr 15
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.283C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.298C>G
  hgvsp: ENSP00000422132.1:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.298C>G
  hgvsp: ENSP00000427582.1:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-39C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.214C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.298C>G
  hgvsp: ENSP00000426154.1:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.206C>G
  hgvsp: ENSP00000421891.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.298C>G
  hgvsp: ENSP00000221214.6:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.470C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.298C>G
  hgvsp: ENSP00000393099.2:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.263C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.298C>G
  hgvsp: ENSP00000397570.2:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.239C>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro100Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

15-42103411-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103411
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103411
    reference: chr 15
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.305G>C
  hgvsp: ENSP00000221214.6:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.305G>C
  hgvsp: ENSP00000393099.2:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.477G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.221G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.305G>C
  hgvsp: ENSP00000397570.2:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-32G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*3G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.305G>C
  hgvsp: ENSP00000426154.1:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.290G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.246G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.305G>C
  hgvsp: ENSP00000427582.1:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.305G>C
  hgvsp: ENSP00000422132.1:p.Gly102Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.270G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly102Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-42103415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103415
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103415
    reference: chr 15
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.481G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.225G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.294G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.309G>A
  hgvsp: ENST00000514566.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.309G>A
  hgvsp: ENST00000512970.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.309G>A
  hgvsp: ENST00000457542.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-28G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.250G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.309G>A
  hgvsp: ENST00000456763.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.309G>A
  hgvsp: ENST00000221214.6:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.309G>A
  hgvsp: ENST00000510535.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.274G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys103Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-42103425-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103425
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103425
    reference: chr 15
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-18A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.319A>G
  hgvsp: ENSP00000397570.2:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.260A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.319A>G
  hgvsp: ENSP00000221214.6:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.319A>G
  hgvsp: ENSP00000393099.2:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.319A>G
  hgvsp: ENSP00000426154.1:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.284A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.235A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.319A>G
  hgvsp: ENSP00000427582.1:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.304A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.319A>G
  hgvsp: ENSP00000422132.1:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*17A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.491A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr107Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

15-42103433-GGTGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103433
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103429
    reference: chr 15
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+6_268+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.249_252delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+6_292+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+6_-10+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+6_312+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+6_*25+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+6_499+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+6_327+9delTGAG
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9511
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.327+6_327+9delTGAG
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: GGTGA
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/15-42103441-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103441
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103441
    reference: chr 15
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.251A>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+8A>C
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.327+8A>C
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-42103452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103452
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103452
    reference: chr 15
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.262T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+19T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+19T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

15-42103453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103453
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103453
    reference: chr 15
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.263G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+20G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+20G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

15-42103460-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103460
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103461
    reference: chr 15
allele count: 7
allele frequency: 5.772148558612046e-5
allele num: 121272
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.271dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+28dupT
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+28dupT
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14879
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9428
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

15-42103467-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103467
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103467
    reference: chr 15
allele count: 3
allele frequency: 2.474145182839329e-5
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.277G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+34G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+34G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9342
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

15-42103469-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103469
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103469
    reference: chr 15
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.279G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+36G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+36G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

15-42103475-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103475
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103475
    reference: chr 15
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.285G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+42G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+42G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

15-42103476-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103476
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103476
    reference: chr 15
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.286T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+43T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+43T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

15-42103482-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103482
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103482
    reference: chr 15
allele count: 2
allele frequency: 1.651336757104876e-5
allele num: 121114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.292G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+49G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12085
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9002
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

15-42103485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103485
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103485
    reference: chr 15
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507147
  gene symbol: MAPKBP1
  hgvsc: ENST00000507147.1:n.295C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.268+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+52C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+52C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

15-42103622-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103622
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103622
    reference: chr 15
allele count: 1
allele frequency: 7.54261577915221e-5
allele num: 13258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+189A>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.269-45A>G
  variant of: http://identifiers.org/hgnc/29536
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

15-42103666-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103666
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103666
    reference: chr 15
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.269-1G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+233G>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.269-1G>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

15-42103679-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103679
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103679
    reference: chr 15
allele count: 1
allele frequency: 8.874689385871494e-5
allele num: 11268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.281A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+246A>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

15-42103709-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103709
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103709
    reference: chr 15
allele count: 2
allele frequency: 1.819836214740673e-4
allele num: 10990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.311C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+276C>G
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

15-42103717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103717
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103717
    reference: chr 15
allele count: 1
allele frequency: 9.137426900584795e-5
allele num: 10944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-10+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*25+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.292+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.319G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.499+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.327+284G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.312+284G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

15-42103809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103809
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103809
    reference: chr 15
allele count: 1
allele frequency: 9.264406151565684e-5
allele num: 10794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.411G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-346G>A
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

15-42103817-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103817
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103817
    reference: chr 15
allele count: 22
allele frequency: 2.037791774731382e-3
allele num: 10796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.419C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-338C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-338C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

15-42103822-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103822
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103822
    reference: chr 15
allele count: 3145
allele frequency: 2.908267061216941e-1
allele num: 10814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.424C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-333C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-333C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 2587
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.5e0
  variant carriers: 335
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 512
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

15-42103825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103825
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103825
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 10798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.427C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-330C>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-330C>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-42103846-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103846
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103846
    reference: chr 15
allele count: 1
allele frequency: 9.266123054114158e-5
allele num: 10792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.448A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-309A>T
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-309A>T
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

15-42103858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42103858
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42103858
    reference: chr 15
allele count: 1
allele frequency: 9.264406151565684e-5
allele num: 10794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000505061
  gene symbol: MAPKBP1
  hgvsc: ENST00000505061.1:n.293-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000397570
  ensembl transcript: ENST00000457542
  gene symbol: MAPKBP1
  hgvsc: ENST00000457542.2:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000221214
  ensembl transcript: ENST00000221214
  gene symbol: MAPKBP1
  hgvsc: ENST00000221214.6:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000515164
  gene symbol: MAPKBP1
  hgvsc: ENST00000515164.1:n.313-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000427582
  ensembl transcript: ENST00000512970
  gene symbol: MAPKBP1
  hgvsc: ENST00000512970.1:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000507762
  gene symbol: MAPKBP1
  hgvsc: ENST00000507762.1:n.460T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000421891
  ensembl transcript: ENST00000505373
  gene symbol: MAPKBP1
  hgvsc: ENST00000505373.1:c.*26-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000393099
  ensembl transcript: ENST00000456763
  gene symbol: MAPKBP1
  hgvsc: ENST00000456763.2:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl transcript: ENST00000502292
  gene symbol: MAPKBP1
  hgvsc: ENST00000502292.1:n.500-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000260357
  ensembl transcript: ENST00000260357
  gene symbol: MAPKBP1
  hgvsc: ENST00000260357.7:c.-9-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000422132
  ensembl transcript: ENST00000510535
  gene symbol: MAPKBP1
  hgvsc: ENST00000510535.1:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137802
  ensembl protein: ENSP00000426154
  ensembl transcript: ENST00000514566
  gene symbol: MAPKBP1
  hgvsc: ENST00000514566.1:c.328-297T>C
  variant of: http://identifiers.org/hgnc/29536
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

GenotypeQuality
all individuals: 22243
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3061
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 649
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4609
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 5.923e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

FS
type: SiteQuality
SIO_000300: 3.078e0

QD
type: SiteQuality
SIO_000300: 1.482e1

DP
type: SiteQuality
SIO_000300: 2.288301e6

GenotypeQuality
all individuals: 22244
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2068
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5540
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 663
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.411e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

DP
type: SiteQuality
SIO_000300: 2.288599e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.963e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2039
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10514
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1032
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1322
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e0

DP
type: SiteQuality
SIO_000300: 2.395967e6

FS
type: SiteQuality
SIO_000300: 1.944e0

QD
type: SiteQuality
SIO_000300: 3.111e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.108e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeDepth
all individuals: 338
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1919
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5373
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15678
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.39705e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e0

QD
type: SiteQuality
SIO_000300: 1.142e1

VQSLOD
type: SiteQuality
SIO_000300: -2.066e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.652e0

GenotypeDepth
all individuals: 1498
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3192
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4210
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3103
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21312
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

African
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allele frequency: 9.611687812379854e-5
allele num: 10404
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South Asian
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Other
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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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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 3.844675124951942e-4
allele num: 10404
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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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
allele num: 66630
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Latino
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QD
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DP
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 7

African
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allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 7.505253677574302e-5
allele num: 66620
num of homozygotes: 0

Other
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European (Finnish)
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num of homozygotes: 0

East Asian
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.24e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

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

South Asian
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African
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allele num: 10396
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66662
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East Asian
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African
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Other
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South Asian
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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South Asian
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European (Finnish)
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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QD
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VQSLOD
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MQ
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MQRankSum
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DP
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
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num of homozygotes: 0

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

Latino
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allele num: 11568
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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South Asian
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

European (Finnish)
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South Asian
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African
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East Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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African
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Other
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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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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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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MQ
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DP
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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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Other
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European (Non-Finnish)
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European (Finnish)
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African
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MQ
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VQSLOD
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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East Asian
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MQ
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BaseQRankSum
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QD
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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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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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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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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FS
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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East Asian
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Latino
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European (Finnish)
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South Asian
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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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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African
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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BaseQRankSum
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MQRankSum
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FS
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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SIO_000300: 1.98e-1

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6348
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 2.5e0
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GenotypeQuality
all individuals: 188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3652
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.662406815761449e-4
allele num: 7512
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.985e0

DP
type: SiteQuality
SIO_000300: 1.59082e5

FS
type: SiteQuality
SIO_000300: 1.599e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.305e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

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

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2836
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.33155792276964e-4
allele num: 7510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.911e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.06e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.934e0

FS
type: SiteQuality
SIO_000300: 1.189e0

DP
type: SiteQuality
SIO_000300: 1.56425e5

QD
type: SiteQuality
SIO_000300: 1.201e1

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 768
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 1

GenotypeQuality
all individuals: 3637
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2748
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.152e0

VQSLOD
type: SiteQuality
SIO_000300: -9.495e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

DP
type: SiteQuality
SIO_000300: 1.48717e5

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

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
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variant carriers: 0

GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 764
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.75e1
variant carriers: 20

South Asian
type: Population
allele count: 19
allele frequency: 2.53130828670397e-3
allele num: 7506
num of homozygotes: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.091703056768559e-3
allele num: 2748
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.697e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.52386e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

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

GenotypeQuality
all individuals: 38
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 16

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 29

GenotypeQuality
all individuals: 121
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variant carriers: 51

GenotypeQuality
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variant carriers: 8

GenotypeQuality
all individuals: 804
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variant carriers: 3

GenotypeQuality
all individuals: 352
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variant carriers: 9

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 89

GenotypeQuality
all individuals: 13
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variant carriers: 13

GenotypeQuality
all individuals: 2327
bin: 7.5e0
variant carriers: 206

GenotypeQuality
all individuals: 89
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variant carriers: 5

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 14

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 21
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variant carriers: 10

GenotypeQuality
all individuals: 7
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variant carriers: 7

GenotypeQuality
all individuals: 99
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variant carriers: 82

GenotypeQuality
all individuals: 79
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2205
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2648
bin: 9.75e1
variant carriers: 2631

Latino
type: Population
allele count: 27
allele frequency: 2.934782608695652e-1
allele num: 92
num of homozygotes: 4

African
type: Population
allele count: 54
allele frequency: 2.755102040816326e-1
allele num: 196
num of homozygotes: 5

East Asian
type: Population
allele count: 3
allele frequency: 2.205882352941177e-2
allele num: 136
num of homozygotes: 0

Other
type: Population
allele count: 29
allele frequency: 2.457627118644068e-1
allele num: 118
num of homozygotes: 5

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

South Asian
type: Population
allele count: 2016
allele frequency: 2.685851318944844e-1
allele num: 7506
num of homozygotes: 309

European (Non-Finnish)
type: Population
allele count: 1016
allele frequency: 3.673174258857556e-1
allele num: 2766
num of homozygotes: 189

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.388e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

DP
type: SiteQuality
SIO_000300: 6.69239e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 0
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 78
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 210
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2754
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.623e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

VQSLOD
type: SiteQuality
SIO_000300: 4.73e-1

DP
type: SiteQuality
SIO_000300: 1.56071e5

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeDepth
all individuals: 8
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variant carriers: 1

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 3847
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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: 140
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 210
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.336e0

QD
type: SiteQuality
SIO_000300: 1.339e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 3.851e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.56351e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 551
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 210
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3982
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2748
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 3.969e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.474e0

DP
type: SiteQuality
SIO_000300: 1.56722e5

VQSLOD
type: SiteQuality
SIO_000300: -2.388e0

QD
type: SiteQuality
SIO_000300: 1.066e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.127e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0