7-151855933-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855933
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855933
    reference: chr 7
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11676+9T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2502T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11670+15T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9190+15T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1428+15T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4186+15T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9387+9T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8890
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

7-151855934-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855934
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855934
    reference: chr 7
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11676+8A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4186+14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1428+14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9387+8A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11670+14A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2503A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9190+14A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15966
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: c.11676+8A>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

7-151855939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855939
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855939
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4186+9G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11670+9G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11676+3G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1428+9G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9387+3G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9190+9G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2508G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3272
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3998
  bin: 8.25e1
  variant carriers: 0
hgvs: c.11676+3G>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-151855946-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855946
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855946
    reference: chr 7
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11670+2T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9190+2T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1428+2T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2515T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4186+2T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9383T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11672T>A
  hgvsp: ENSP00000347325.2:p.Val3891Glu
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: c.11670+2T>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-151855952-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855952
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855952
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9186A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2521A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11666A>G
  hgvsp: ENSP00000347325.2:p.Lys3889Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4182A>G
  hgvsp: ENSP00000353218.3:p.Lys1395Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11666A>G
  hgvsp: ENSP00000262189.6:p.Lys3889Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9377A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1424A>G
  hgvsp: ENSP00000410411.1:p.Lys475Arg
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12025
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3997
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys3889Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-151855953-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855953
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855953
    reference: chr 7
allele count: 9
allele frequency: 7.412776331828814e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11665A>C
  hgvsp: ENSP00000262189.6:p.Lys3889Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9376A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11665A>C
  hgvsp: ENSP00000347325.2:p.Lys3889Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1423A>C
  hgvsp: ENSP00000410411.1:p.Lys475Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4181A>C
  hgvsp: ENSP00000353218.3:p.Lys1395Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2522A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9185A>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys3889Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/7-151855956-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855956
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855956
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9373T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11662T>G
  hgvsp: ENSP00000347325.2:p.Leu3888Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2525T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11662T>G
  hgvsp: ENSP00000262189.6:p.Leu3888Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9182T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1420T>G
  hgvsp: ENSP00000410411.1:p.Leu474Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4178T>G
  hgvsp: ENSP00000353218.3:p.Leu1394Val
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5109
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12018
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu3888Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

7-151855958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855958
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855958
    reference: chr 7
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2527A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11660A>G
  hgvsp: ENSP00000347325.2:p.His3887Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4176A>G
  hgvsp: ENSP00000353218.3:p.His1393Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9180A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1418A>G
  hgvsp: ENSP00000410411.1:p.His473Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11660A>G
  hgvsp: ENSP00000262189.6:p.His3887Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9371A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2876
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22720
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His3887Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-151855966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855966
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855966
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9172G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2535G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11652G>A
  hgvsp: ENST00000262189.6:c.11652G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9363G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4168G>A
  hgvsp: ENST00000360104.3:c.4168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11652G>A
  hgvsp: ENST00000355193.2:c.11652G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1410G>A
  hgvsp: ENST00000424877.1:c.1410G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12015
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2877
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr3884Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

7-151855967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855967
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855967
    reference: chr 7
allele count: 7
allele frequency: 5.765492702533522e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9171C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9362C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4167C>T
  hgvsp: ENSP00000353218.3:p.Thr1390Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1409C>T
  hgvsp: ENSP00000410411.1:p.Thr470Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11651C>T
  hgvsp: ENSP00000347325.2:p.Thr3884Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11651C>T
  hgvsp: ENSP00000262189.6:p.Thr3884Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2536C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr3884Met
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-151855968-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855968
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855968
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4166A>T
  hgvsp: ENSP00000353218.3:p.Thr1390Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9170A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11650A>T
  hgvsp: ENSP00000347325.2:p.Thr3884Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2537A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1408A>T
  hgvsp: ENSP00000410411.1:p.Thr470Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9361A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11650A>T
  hgvsp: ENSP00000262189.6:p.Thr3884Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12008
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr3884Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

7-151855972-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855972
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855972
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11646T>A
  hgvsp: ENST00000355193.2:c.11646T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9357T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2541T>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11646T>A
  hgvsp: ENST00000262189.6:c.11646T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1404T>A
  hgvsp: ENST00000424877.1:c.1404T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4162T>A
  hgvsp: ENST00000360104.3:c.4162T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9166T>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12008
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22725
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr3882Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-151855979-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855979
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855979
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11639C>A
  hgvsp: ENSP00000262189.6:p.Ser3880Tyr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1397C>A
  hgvsp: ENSP00000410411.1:p.Ser466Tyr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11639C>A
  hgvsp: ENSP00000347325.2:p.Ser3880Tyr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2548C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9350C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4155C>A
  hgvsp: ENSP00000353218.3:p.Ser1386Tyr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9159C>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser3880Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

7-151855982-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855982
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855982
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11636A>G
  hgvsp: ENSP00000262189.6:p.Tyr3879Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9156A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4152A>G
  hgvsp: ENSP00000353218.3:p.Tyr1385Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1394A>G
  hgvsp: ENSP00000410411.1:p.Tyr465Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2551A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11636A>G
  hgvsp: ENSP00000347325.2:p.Tyr3879Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9347A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr3879Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

7-151855983-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855983
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855983
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11635T>C
  hgvsp: ENSP00000262189.6:p.Tyr3879His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9346T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4151T>C
  hgvsp: ENSP00000353218.3:p.Tyr1385His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2552T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9155T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1393T>C
  hgvsp: ENSP00000410411.1:p.Tyr465His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11635T>C
  hgvsp: ENSP00000347325.2:p.Tyr3879His
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr3879His
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

7-151855986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855986
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855986
    reference: chr 7
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4148A>G
  hgvsp: ENSP00000353218.3:p.Met1384Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9343A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9152A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11632A>G
  hgvsp: ENSP00000347325.2:p.Met3878Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1390A>G
  hgvsp: ENSP00000410411.1:p.Met464Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11632A>G
  hgvsp: ENSP00000262189.6:p.Met3878Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2555A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12006
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4002
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met3878Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-151855999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855999
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855999
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9139G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1377G>A
  hgvsp: ENST00000424877.1:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4135G>A
  hgvsp: ENST00000360104.3:c.4135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11619G>A
  hgvsp: ENST00000262189.6:c.11619G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9330G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11619G>A
  hgvsp: ENST00000355193.2:c.11619G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2568G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu3873Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-151855999-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151855999
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151855996
    reference: chr 7
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2571_49-2569delAGA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9327_9329delAGA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1374_1376delAGA
  hgvsp: ENSP00000410411.1:p.Glu460del
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11616_11618delAGA
  hgvsp: ENSP00000347325.2:p.Glu3874del
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4132_4134delAGA
  hgvsp: ENSP00000353218.3:p.Glu1380del
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11616_11618delAGA
  hgvsp: ENSP00000262189.6:p.Glu3874del
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9136_*9138delAGA
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4002
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu3874del
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: CTCT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

7-151856001-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856001
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856001
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11617G>C
  hgvsp: ENSP00000262189.6:p.Glu3873Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9328G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11617G>C
  hgvsp: ENSP00000347325.2:p.Glu3873Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1375G>C
  hgvsp: ENSP00000410411.1:p.Glu459Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2570G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4133G>C
  hgvsp: ENSP00000353218.3:p.Glu1379Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9137G>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu3873Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

7-151856004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856004
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856004
    reference: chr 7
allele count: 110
allele frequency: 9.060059961124106e-4
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2573G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1372G>A
  hgvsp: ENSP00000410411.1:p.Glu458Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4130G>A
  hgvsp: ENSP00000353218.3:p.Glu1378Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11614G>A
  hgvsp: ENSP00000347325.2:p.Glu3872Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9325G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11614G>A
  hgvsp: ENSP00000262189.6:p.Glu3872Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9134G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 9.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5109
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu3872Lys
num of homozygotes: 1
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

7-151856005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856005
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856005
    reference: chr 7
allele count: 6
allele frequency: 4.941932295527551e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1371C>T
  hgvsp: ENST00000424877.1:c.1371C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11613C>T
  hgvsp: ENST00000262189.6:c.11613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4129C>T
  hgvsp: ENST00000360104.3:c.4129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11613C>T
  hgvsp: ENST00000355193.2:c.11613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9324C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2574C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9133C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp3871Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

7-151856008-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856008
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856007
    reference: chr 7
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9320delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9129delA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4125delA
  hgvsp: ENSP00000353218.3:p.Lys1376ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11609delA
  hgvsp: ENSP00000347325.2:p.Lys3870ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11609delA
  hgvsp: ENSP00000262189.6:p.Lys3870ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1367delA
  hgvsp: ENSP00000410411.1:p.Lys456ArgfsTer19
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2578delA
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11942
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3278
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys3870ArgfsTer19
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: CT
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

7-151856011-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856011
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856011
    reference: chr 7
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4123A>G
  hgvsp: ENST00000360104.3:c.4123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11607A>G
  hgvsp: ENST00000262189.6:c.11607A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1365A>G
  hgvsp: ENST00000424877.1:c.1365A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9127A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11607A>G
  hgvsp: ENST00000355193.2:c.11607A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9318A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2580A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys3869Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

7-151856016-TTTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856016
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856012
    reference: chr 7
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11598_11601delGAAA
  hgvsp: ENSP00000347325.2:p.Lys3867GlyfsTer21
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1356_1359delGAAA
  hgvsp: ENSP00000410411.1:p.Lys453GlyfsTer21
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11598_11601delGAAA
  hgvsp: ENSP00000262189.6:p.Lys3867GlyfsTer21
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9309_9312delGAAA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4114_4117delGAAA
  hgvsp: ENSP00000353218.3:p.Lys1373GlyfsTer21
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9118_*9121delGAAA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2589_49-2586delGAAA
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys3867GlyfsTer21
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TTTTC
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-151856027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856027
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856027
    reference: chr 7
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2596G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1349G>A
  hgvsp: ENSP00000410411.1:p.Arg450His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4107G>A
  hgvsp: ENSP00000353218.3:p.Arg1370His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11591G>A
  hgvsp: ENSP00000347325.2:p.Arg3864His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11591G>A
  hgvsp: ENSP00000262189.6:p.Arg3864His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9111G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9302G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11939
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg3864His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-151856028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856028
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856028
    reference: chr 7
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9301C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9110C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11590C>T
  hgvsp: ENSP00000347325.2:p.Arg3864Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1348C>T
  hgvsp: ENSP00000410411.1:p.Arg450Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11590C>T
  hgvsp: ENSP00000262189.6:p.Arg3864Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4106C>T
  hgvsp: ENSP00000353218.3:p.Arg1370Cys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2597C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg3864Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-151856036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856036
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856036
    reference: chr 7
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11582C>T
  hgvsp: ENSP00000347325.2:p.Ala3861Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2605C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11582C>T
  hgvsp: ENSP00000262189.6:p.Ala3861Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9102C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9293C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1340C>T
  hgvsp: ENSP00000410411.1:p.Ala447Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4098C>T
  hgvsp: ENSP00000353218.3:p.Ala1367Val
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala3861Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

7-151856043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856043
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856043
    reference: chr 7
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1333G>A
  hgvsp: ENSP00000410411.1:p.Glu445Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11575G>A
  hgvsp: ENSP00000347325.2:p.Glu3859Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2612G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9095G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4091G>A
  hgvsp: ENSP00000353218.3:p.Glu1365Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11575G>A
  hgvsp: ENSP00000262189.6:p.Glu3859Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9286G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu3859Lys
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-151856047-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856047
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856047
    reference: chr 7
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11571G>C
  hgvsp: ENST00000355193.2:c.11571G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9091G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11571G>C
  hgvsp: ENST00000262189.6:c.11571G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1329G>C
  hgvsp: ENST00000424877.1:c.1329G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2616G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9282G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4087G>C
  hgvsp: ENST00000360104.3:c.4087G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11931
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr3857Thr
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

7-151856047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856047
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856047
    reference: chr 7
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4087G>A
  hgvsp: ENST00000360104.3:c.4087G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11571G>A
  hgvsp: ENST00000262189.6:c.11571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9282G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9091G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11571G>A
  hgvsp: ENST00000355193.2:c.11571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2616G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1329G>A
  hgvsp: ENST00000424877.1:c.1329G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11931
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22762
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8906
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr3857Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-151856048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856048
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856048
    reference: chr 7
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11570C>T
  hgvsp: ENSP00000262189.6:p.Thr3857Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1328C>T
  hgvsp: ENSP00000410411.1:p.Thr443Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11570C>T
  hgvsp: ENSP00000347325.2:p.Thr3857Met
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2617C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9090C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9281C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4086C>T
  hgvsp: ENSP00000353218.3:p.Thr1363Met
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11926
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr3857Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

7-151856049-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856049
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856049
    reference: chr 7
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1327A>T
  hgvsp: ENSP00000410411.1:p.Thr443Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2618A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11569A>T
  hgvsp: ENSP00000262189.6:p.Thr3857Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9280A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11569A>T
  hgvsp: ENSP00000347325.2:p.Thr3857Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9089A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4085A>T
  hgvsp: ENSP00000353218.3:p.Thr1363Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr3857Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

7-151856053-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856053
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856053
    reference: chr 7
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4081G>C
  hgvsp: ENSP00000353218.3:p.Gln1361His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9085G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11565G>C
  hgvsp: ENSP00000262189.6:p.Gln3855His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1323G>C
  hgvsp: ENSP00000410411.1:p.Gln441His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2622G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11565G>C
  hgvsp: ENSP00000347325.2:p.Gln3855His
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9276G>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln3855His
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

7-151856060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856060
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856060
    reference: chr 7
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2629G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4074G>A
  hgvsp: ENSP00000353218.3:p.Arg1359Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1316G>A
  hgvsp: ENSP00000410411.1:p.Arg439Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11558G>A
  hgvsp: ENSP00000262189.6:p.Arg3853Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9078G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9269G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11558G>A
  hgvsp: ENSP00000347325.2:p.Arg3853Gln
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22770
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg3853Gln
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

7-151856062-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856062
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856062
    reference: chr 7
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4072A>G
  hgvsp: ENST00000360104.3:c.4072A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2631A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11556A>G
  hgvsp: ENST00000262189.6:c.11556A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9076A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1314A>G
  hgvsp: ENST00000424877.1:c.1314A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11556A>G
  hgvsp: ENST00000355193.2:c.11556A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9267A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys3852Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

7-151856069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856069
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856069
    reference: chr 7
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11549G>A
  hgvsp: ENSP00000347325.2:p.Arg3850Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11549G>A
  hgvsp: ENSP00000262189.6:p.Arg3850Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9260G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4065G>A
  hgvsp: ENSP00000353218.3:p.Arg1356Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1307G>A
  hgvsp: ENSP00000410411.1:p.Arg436Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9069G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2638G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg3850Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-151856076-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856076
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856076
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9253A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4058A>C
  hgvsp: ENSP00000353218.3:p.Lys1354Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1300A>C
  hgvsp: ENSP00000410411.1:p.Lys434Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9062A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11542A>C
  hgvsp: ENSP00000347325.2:p.Lys3848Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11542A>C
  hgvsp: ENSP00000262189.6:p.Lys3848Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2645A>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys3848Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/7-151856077-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856077
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856077
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2646G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1299G>T
  hgvsp: ENSP00000410411.1:p.Lys433Asn
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4057G>T
  hgvsp: ENSP00000353218.3:p.Lys1353Asn
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11541G>T
  hgvsp: ENSP00000262189.6:p.Lys3847Asn
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11541G>T
  hgvsp: ENSP00000347325.2:p.Lys3847Asn
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9061G>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9252G>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22773
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys3847Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-151856080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856080
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856080
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11538C>T
  hgvsp: ENST00000262189.6:c.11538C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11538C>T
  hgvsp: ENST00000355193.2:c.11538C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9249C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4054C>T
  hgvsp: ENST00000360104.3:c.4054C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9058C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1296C>T
  hgvsp: ENST00000424877.1:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2649C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr3846Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

7-151856084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856084
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856084
    reference: chr 7
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4050A>G
  hgvsp: ENSP00000353218.3:p.Glu1351Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9054A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11534A>G
  hgvsp: ENSP00000347325.2:p.Glu3845Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11534A>G
  hgvsp: ENSP00000262189.6:p.Glu3845Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2653A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1292A>G
  hgvsp: ENSP00000410411.1:p.Glu431Gly
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9245A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu3845Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

7-151856090-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856090
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856090
    reference: chr 7
allele count: 38
allele frequency: 3.130199838547587e-4
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2659G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4044G>C
  hgvsp: ENSP00000353218.3:p.Gly1349Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11528G>C
  hgvsp: ENSP00000347325.2:p.Gly3843Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11528G>C
  hgvsp: ENSP00000262189.6:p.Gly3843Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9048G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9239G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1286G>C
  hgvsp: ENSP00000410411.1:p.Gly429Ala
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly3843Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-151856096-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856096
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856096
    reference: chr 7
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11522A>T
  hgvsp: ENSP00000347325.2:p.Asp3841Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11522A>T
  hgvsp: ENSP00000262189.6:p.Asp3841Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4038A>T
  hgvsp: ENSP00000353218.3:p.Asp1347Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9042A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1280A>T
  hgvsp: ENSP00000410411.1:p.Asp427Val
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2665A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9233A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11892
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp3841Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

7-151856098-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856098
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856098
    reference: chr 7
allele count: 7
allele frequency: 5.766062602965403e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1278A>T
  hgvsp: ENST00000424877.1:c.1278A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4036A>T
  hgvsp: ENST00000360104.3:c.4036A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11520A>T
  hgvsp: ENST00000355193.2:c.11520A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2667A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9040A>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11520A>T
  hgvsp: ENST00000262189.6:c.11520A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9231A>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22790
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr3840Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

7-151856103-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856103
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856103
    reference: chr 7
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9226A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4031A>C
  hgvsp: ENSP00000353218.3:p.Lys1345Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11515A>C
  hgvsp: ENSP00000347325.2:p.Lys3839Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11515A>C
  hgvsp: ENSP00000262189.6:p.Lys3839Gln
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9035A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2672A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1273A>C
  hgvsp: ENSP00000410411.1:p.Lys425Gln
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22794
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys3839Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-151856106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856106
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856106
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2675C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9223C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4028C>T
  hgvsp: ENSP00000353218.3:p.Pro1344Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11512C>T
  hgvsp: ENSP00000262189.6:p.Pro3838Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9032C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1270C>T
  hgvsp: ENSP00000410411.1:p.Pro424Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11512C>T
  hgvsp: ENSP00000347325.2:p.Pro3838Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro3838Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

7-151856107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856107
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856107
    reference: chr 7
allele count: 5
allele frequency: 4.11868399808893e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4027G>A
  hgvsp: ENST00000360104.3:c.4027G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1269G>A
  hgvsp: ENST00000424877.1:c.1269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9222G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2676G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9031G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11511G>A
  hgvsp: ENST00000262189.6:c.11511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11511G>A
  hgvsp: ENST00000355193.2:c.11511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu3837Leu
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-151856110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856110
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856110
    reference: chr 7
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2679G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11508G>A
  hgvsp: ENST00000355193.2:c.11508G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4024G>A
  hgvsp: ENST00000360104.3:c.4024G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9028G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1266G>A
  hgvsp: ENST00000424877.1:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11508G>A
  hgvsp: ENST00000262189.6:c.11508G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9219G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11888
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22802
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln3836Gln
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

7-151856111-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856111
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856111
    reference: chr 7
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2680A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11507A>C
  hgvsp: ENSP00000347325.2:p.Gln3836Pro
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4023A>C
  hgvsp: ENSP00000353218.3:p.Gln1342Pro
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11507A>C
  hgvsp: ENSP00000262189.6:p.Gln3836Pro
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9027A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9218A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1265A>C
  hgvsp: ENSP00000410411.1:p.Gln422Pro
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22805
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln3836Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-151856112-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856112
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856112
    reference: chr 7
allele count: 71
allele frequency: 5.848338577618161e-4
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11506C>A
  hgvsp: ENSP00000262189.6:p.Gln3836Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4022C>A
  hgvsp: ENSP00000353218.3:p.Gln1342Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11506C>A
  hgvsp: ENSP00000347325.2:p.Gln3836Lys
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9026C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2681C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9217C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1264C>A
  hgvsp: ENSP00000410411.1:p.Gln422Lys
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 16021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22798
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln3836Lys
num of homozygotes: 1
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

7-151856117-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856117
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856117
    reference: chr 7
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9212G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4017G>C
  hgvsp: ENSP00000353218.3:p.Gly1340Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11501G>C
  hgvsp: ENSP00000262189.6:p.Gly3834Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11501G>C
  hgvsp: ENSP00000347325.2:p.Gly3834Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1259G>C
  hgvsp: ENSP00000410411.1:p.Gly420Ala
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9021G>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2686G>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3278
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11844
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4009
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly3834Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

7-151856119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856119
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856119
    reference: chr 7
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11499T>C
  hgvsp: ENST00000262189.6:c.11499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11499T>C
  hgvsp: ENST00000355193.2:c.11499T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9210T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1257T>C
  hgvsp: ENST00000424877.1:c.1257T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9019T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4015T>C
  hgvsp: ENST00000360104.3:c.4015T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2688T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys3833Cys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

7-151856121-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856121
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856121
    reference: chr 7
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9208T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11497T>C
  hgvsp: ENSP00000262189.6:p.Cys3833Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1255T>C
  hgvsp: ENSP00000410411.1:p.Cys419Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4013T>C
  hgvsp: ENSP00000353218.3:p.Cys1339Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11497T>C
  hgvsp: ENSP00000347325.2:p.Cys3833Arg
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2690T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9017T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys3833Arg
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

7-151856132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856132
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856132
    reference: chr 7
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1244G>A
  hgvsp: ENSP00000410411.1:p.Gly415Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9006G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2701G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11486G>A
  hgvsp: ENSP00000347325.2:p.Gly3829Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4002G>A
  hgvsp: ENSP00000353218.3:p.Gly1335Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9197G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11486G>A
  hgvsp: ENSP00000262189.6:p.Gly3829Asp
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4009
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11841
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly3829Asp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

7-151856133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856133
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856133
    reference: chr 7
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.4001G>A
  hgvsp: ENSP00000353218.3:p.Gly1335Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*9005G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1243G>A
  hgvsp: ENSP00000410411.1:p.Gly415Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11485G>A
  hgvsp: ENSP00000262189.6:p.Gly3829Ser
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2702G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9196G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11485G>A
  hgvsp: ENSP00000347325.2:p.Gly3829Ser
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11838
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly3829Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

7-151856145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856145
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856145
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2714G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3989G>A
  hgvsp: ENSP00000353218.3:p.Ala1331Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11473G>A
  hgvsp: ENSP00000347325.2:p.Ala3825Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11473G>A
  hgvsp: ENSP00000262189.6:p.Ala3825Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9184G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1231G>A
  hgvsp: ENSP00000410411.1:p.Ala411Thr
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8993G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala3825Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

7-151856151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856151
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856151
    reference: chr 7
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2720T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11467T>C
  hgvsp: ENST00000355193.2:c.11467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11467T>C
  hgvsp: ENST00000262189.6:c.11467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8987T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3983T>C
  hgvsp: ENST00000360104.3:c.3983T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1225T>C
  hgvsp: ENST00000424877.1:c.1225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9178T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8899
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5117
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu3823Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

7-151856160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856160
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856160
    reference: chr 7
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9172-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11461-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2729T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8981-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11461-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1219-3T>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3977-3T>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16016
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11830
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: c.11461-3T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

7-151856184-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856184
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856184
    reference: chr 7
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8981-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9172-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11461-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11461-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3977-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1219-27A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2753A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15414
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/7-151856194-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856194
    reference: chr 7
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11461-37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11461-37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8981-37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1219-37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2763T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3977-37T>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9172-37T>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11813
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-151856207-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856207
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856207
    reference: chr 7
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1219-50C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11461-50C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8981-50C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11461-50C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3977-50C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2776C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9172-50C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

7-151856208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151856208
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151856208
    reference: chr 7
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3977-51A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1219-51A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.49-2777A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9172-51A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11461-51A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11461-51A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8981-51A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3893
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3761
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2716
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

7-151859152-ATAATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859152
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859147
    reference: chr 7
allele count: 6
allele frequency: 5.903303882406187e-5
allele num: 101638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+45_3976+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+45_1218+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+45_*8980+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+45_9171+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+45_11460+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+45_11460+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+45_48+49delAATTA
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11443
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4457
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: ATAATT
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

7-151859158-TAAAAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859158
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859153
    reference: chr 7
allele count: 1
allele frequency: 9.824147755182238e-6
allele num: 101790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+39_11460+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+39_11460+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+39_9171+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+39_1218+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+39_*8980+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+39_48+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+39_3976+43delGTTTT
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3360
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5277
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: TAAAAC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

7-151859177-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859177
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859177
    reference: chr 7
allele count: 1
allele frequency: 9.62982935942375e-6
allele num: 103844
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+25A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+25A>C
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28246
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3629
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

7-151859180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859180
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859180
    reference: chr 7
allele count: 4
allele frequency: 3.833988306335666e-5
allele num: 104330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+22G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+22G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10215
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3584
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4127
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-151859181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859181
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859181
    reference: chr 7
allele count: 3
allele frequency: 2.865657955066483e-5
allele num: 104688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+21C>T
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+21C>T
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4358
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-151859186-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859186
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859186
    reference: chr 7
allele count: 18
allele frequency: 1.702288632494798e-4
allele num: 105740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+16A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+16A>G
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 3155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-151859189-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859189
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859189
    reference: chr 7
allele count: 1
allele frequency: 9.407337723424271e-6
allele num: 106300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+13C>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+13C>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

7-151859193-T-TAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859193
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859195
    reference: chr 7
allele count: 1
allele frequency: 9.350513343182541e-6
allele num: 106946
alternate allele: TAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+7_11460+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+7_*8980+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+7_48+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+7_3976+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+7_11460+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+7_9171+8dupGT
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+7_1218+8dupGT
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3586
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4630
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-151859197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859197
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859197
    reference: chr 7
allele count: 1
allele frequency: 9.302671727320086e-6
allele num: 107496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1218+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9171+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8980+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11460+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11460+5G>A
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3976+5G>A
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3587
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
hgvs: c.11460+5G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

7-151859205-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859205
    reference: chr 7
allele count: 1
allele frequency: 9.205390676780322e-6
allele num: 108632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9168A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11457A>C
  hgvsp: ENST00000355193.2:c.11457A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1215A>C
  hgvsp: ENST00000424877.1:c.1215A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3973A>C
  hgvsp: ENST00000360104.3:c.3973A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8977A>C
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11457A>C
  hgvsp: ENST00000262189.6:c.11457A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.45A>C
  hgvsp: ENST00000418061.1:c.45A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly3819Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

7-151859219-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 151859219
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 151859219
    reference: chr 7
allele count: 5
allele frequency: 4.543802253725918e-5
allele num: 110040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000353218
  ensembl transcript: ENST00000360104
  gene symbol: KMT2C
  hgvsc: ENST00000360104.3:c.3959A>G
  hgvsp: ENSP00000353218.3:p.Asn1321Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000055609
  ensembl transcript: ENST00000473186
  gene symbol: KMT2C
  hgvsc: ENST00000473186.1:n.9154A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000347325
  ensembl transcript: ENST00000355193
  gene symbol: KMT2C
  hgvsc: ENST00000355193.2:c.11443A>G
  hgvsp: ENSP00000347325.2:p.Asn3815Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000453752
  ensembl transcript: ENST00000558084
  gene symbol: KMT2C
  hgvsc: ENST00000558084.1:c.*8963A>G
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000262189
  ensembl transcript: ENST00000262189
  gene symbol: KMT2C
  hgvsc: ENST00000262189.6:c.11443A>G
  hgvsp: ENSP00000262189.6:p.Asn3815Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000408001
  ensembl transcript: ENST00000418061
  gene symbol: KMT2C
  hgvsc: ENST00000418061.1:c.31A>G
  hgvsp: ENSP00000408001.1:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/13726
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000055609
  ensembl protein: ENSP00000410411
  ensembl transcript: ENST00000424877
  gene symbol: KMT2C
  hgvsc: ENST00000424877.1:c.1201A>G
  hgvsp: ENSP00000410411.1:p.Asn401Asp
  variant of: http://identifiers.org/hgnc/13726
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn3815Asp
num of homozygotes: 0
reference allele: T

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

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12028
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5110
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.608e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.837e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

FS
type: SiteQuality
SIO_000300: 1.769e0

DP
type: SiteQuality
SIO_000300: 2.274179e6

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12029
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8890
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22694
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.706e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.99e-1

DP
type: SiteQuality
SIO_000300: 2.27445e6

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.145e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22704
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8890
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5110
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: -1.518e0

VQSLOD
type: SiteQuality
SIO_000300: -6.805e-1

DP
type: SiteQuality
SIO_000300: 2.27392e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e0

GenotypeQuality
all individuals: 1812
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3997
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2874
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

FS
type: SiteQuality
SIO_000300: 7.299e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 2.273854e6

VQSLOD
type: SiteQuality
SIO_000300: -6.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

QD
type: SiteQuality
SIO_000300: 1.608e1

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

GenotypeQuality
all individuals: 1812
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8891
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.456e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.273913e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.74e-1

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

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

GenotypeQuality
all individuals: 22719
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8891
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3997
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12024
bin: 9.75e1
variant carriers: 9

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.039981511439797e-3
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.275084e6

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

FS
type: SiteQuality
SIO_000300: 1.105e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.27e0

QD
type: SiteQuality
SIO_000300: 1.406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22721
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1813
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.368e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 2.272186e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.407e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e0

GenotypeQuality
all individuals: 5110
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12017
bin: 9.75e1
variant carriers: 3

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

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

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

GenotypeQuality
all individuals: 1813
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 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: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.424e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

FS
type: SiteQuality
SIO_000300: 2.464e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 2.27243e6

MQ
type: SiteQuality
SIO_000300: 5.88e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 3275
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22723
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8891
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5109
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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Latino
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QD
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FS
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10406
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.816860465116279e-4
allele num: 16512
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Other
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Latino
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allele num: 11578
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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DP
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QD
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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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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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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allele num: 66740
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Other
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South Asian
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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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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Other
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East Asian
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African
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Latino
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
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European (Finnish)
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South Asian
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VQSLOD
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FS
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

VQSLOD
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -4.0e-4

MQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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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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variant carriers: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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Other
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 6.056201550387597e-5
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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Latino
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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allele num: 10406
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East Asian
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Other
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VQSLOD
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ReadPosRankSum
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FS
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DP
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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East Asian
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Other
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African
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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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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East Asian
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Other
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European (Non-Finnish)
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Latino
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South Asian
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African
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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African
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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FS
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DP
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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MQ
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VQSLOD
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QD
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DP
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FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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Other
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FS
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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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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GenotypeQuality
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Latino
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.275e0

MQRankSum
type: SiteQuality
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DP
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VQSLOD
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FS
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ClippingRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -9.04e-1

ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
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allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

African
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 5.74e-1

BaseQRankSum
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SIO_000300: 4.96e0

QD
type: SiteQuality
SIO_000300: 1.564e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.683e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.259535e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.662e0

QD
type: SiteQuality
SIO_000300: 1.411e1

MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.106e0

FS
type: SiteQuality
SIO_000300: 6.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.279e1

DP
type: SiteQuality
SIO_000300: 2.25919e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 908
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.258873e6

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
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MQ
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

MQ
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SIO_000300: 5.975e1

ReadPosRankSum
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SIO_000300: 1.11e0

ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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DP
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SIO_000300: 2.258841e6

BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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Other
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FS
type: SiteQuality
SIO_000300: 7.12e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 2.25859e6

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

East Asian
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Other
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African
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South Asian
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allele num: 16510
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 6614
num of homozygotes: 0

European (Non-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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num of homozygotes: 0

South Asian
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allele num: 16510
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Other
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InbreedingCoeff
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SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

FS
type: SiteQuality
SIO_000300: 3.215e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 2.258255e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.325e0

FS
type: SiteQuality
SIO_000300: 3.5997e1

QD
type: SiteQuality
SIO_000300: 5.12e0

BaseQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.722e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 2.25804e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.116e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.7876e1

DP
type: SiteQuality
SIO_000300: 2.258057e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.233e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

FS
type: SiteQuality
SIO_000300: 1.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

DP
type: SiteQuality
SIO_000300: 2.257813e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.345220257716512e-4
allele num: 66740
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
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allele count: 8
allele frequency: 6.916825177243646e-4
allele num: 11566
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.348e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.259366e6

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.48e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.71e0

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 2.255633e6

GenotypeQuality
all individuals: 11891
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491759065028469e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.81e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.89e-1

MQRankSum
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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South Asian
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allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.254479e6

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.63e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
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South Asian
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allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 1.18e0

VQSLOD
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SIO_000300: 1.07e0

BaseQRankSum
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SIO_000300: -5.165e0

FS
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SIO_000300: 2.886e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

MQRankSum
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SIO_000300: -1.289e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
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QD
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FS
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SIO_000300: 3.026e0

BaseQRankSum
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SIO_000300: -2.612e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 2.253851e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 69
allele frequency: 4.179285281647486e-3
allele num: 16510
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

QD
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VQSLOD
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SIO_000300: 4.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

ReadPosRankSum
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SIO_000300: 3.97e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 3.35e-1

DP
type: SiteQuality
SIO_000300: 2.256862e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

GenotypeQuality
all individuals: 2881
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 2.083e0

QD
type: SiteQuality
SIO_000300: 1.192e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.2505e6

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

FS
type: SiteQuality
SIO_000300: 5.51e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

DP
type: SiteQuality
SIO_000300: 2.250524e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

DP
type: SiteQuality
SIO_000300: 2.25033e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.799e0

QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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South Asian
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VQSLOD
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MQ
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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DP
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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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East Asian
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num of homozygotes: 0

Other
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Latino
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African
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European (Non-Finnish)
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allele num: 66734
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European (Finnish)
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South Asian
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 3.9e-3

FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.28e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.052e0

QD
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SIO_000300: 1.514e1

VQSLOD
type: SiteQuality
SIO_000300: -1.63e0

DP
type: SiteQuality
SIO_000300: 2.249039e6

MQRankSum
type: SiteQuality
SIO_000300: -1.574e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.467e1

FS
type: SiteQuality
SIO_000300: 1.993e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.247917e6

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.809e1

VQSLOD
type: SiteQuality
SIO_000300: -8.723e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

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

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

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

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16476
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East Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.807e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.161406e6

QD
type: SiteQuality
SIO_000300: 1.679e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509433962264151e-5
allele num: 66250
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
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: 902
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.508e1

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

DP
type: SiteQuality
SIO_000300: 2.113369e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509661835748792e-5
allele num: 66240
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.367e0

VQSLOD
type: SiteQuality
SIO_000300: -7.756999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.888e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.09e-1

DP
type: SiteQuality
SIO_000300: 2.112119e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 6.287726358148893e-4
allele num: 7952
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.715618995333516e-5
allele num: 58288
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.59e-1

ClippingRankSum
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SIO_000300: 4.7e-2

VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.415e1

MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10906
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.712974065572647e-5
allele num: 58378
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.228501228501228e-4
allele num: 8140
num of homozygotes: 0

European (Finnish)
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Other
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Latino
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 59716
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 6.660228445835692e-5
allele num: 60058
num of homozygotes: 0

African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
type: Population
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Other
type: Population
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allele frequency: 0.0e0
allele num: 750
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33673
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.975784515358588e-5
allele num: 60292
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.345359e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.67e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 1.037e0

VQSLOD
type: SiteQuality
SIO_000300: -1.347e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.287e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

GenotypeQuality
all individuals: 223
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63826998689384e-5
allele num: 61040
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9416
num of homozygotes: 0

East Asian
type: Population
allele count: 17
allele frequency: 2.053636143996134e-3
allele num: 8278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

FS
type: SiteQuality
SIO_000300: 6.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.369489e6

GenotypeQuality
all individuals: 1537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 1.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.059322033898305e-4
allele num: 9440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61412
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.751e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 1.38263e6

FS
type: SiteQuality
SIO_000300: 1.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.53e0

MQRankSum
type: SiteQuality
SIO_000300: -9.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

GenotypeQuality
all individuals: 259
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.617076326002587e-5
allele num: 61840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8712
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

DP
type: SiteQuality
SIO_000300: 1.394051e6

MQ
type: SiteQuality
SIO_000300: 6.016e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

QD
type: SiteQuality
SIO_000300: 1.658e1

GenotypeQuality
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4698
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608130708864017e-5
allele num: 62184
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.405597e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.04e-1

GenotypeQuality
all individuals: 38666
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4340
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.101564221194096e-4
allele num: 9078
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.84e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 5.845e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.175e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.19e-1

FS
type: SiteQuality
SIO_000300: 2.515e0

DP
type: SiteQuality
SIO_000300: 1.422869e6