10-21827718-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827718
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827717
    reference: chr 10
allele count: 1
allele frequency: 8.368901163277262e-6
allele num: 119490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+3987delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-42delT
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: GT
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/10-21827721-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827721
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827721
    reference: chr 10
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+3988C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-41C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-41C>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-21827724-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827724
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827724
    reference: chr 10
allele count: 1
allele frequency: 8.358688020328329e-6
allele num: 119636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+3991C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-38C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-38C>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-21827725-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827725
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827725
    reference: chr 10
allele count: 4
allele frequency: 3.340180703776074e-5
allele num: 119754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+3992G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-37G>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-37G>C
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

10-21827730-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827730
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827730
    reference: chr 10
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+3997T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-32T>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-32T>G
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/10-21827749-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827749
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827749
    reference: chr 10
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4016C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-13C>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

10-21827751-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827751
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827751
    reference: chr 10
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.188-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4018T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.57-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.104-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.192-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.57-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.57-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.161-11T>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16517
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

10-21827781-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827781
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827781
    reference: chr 10
allele count: 5
allele frequency: 4.119905736556747e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.76A>G
  hgvsp: ENST00000430455.1:c.76A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.207A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.180A>G
  hgvsp: ENST00000307729.7:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4048A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.180A>G
  hgvsp: ENST00000377091.2:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.180A>G
  hgvsp: ENST00000377072.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.211A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.180A>G
  hgvsp: ENST00000446906.2:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.180A>G
  hgvsp: ENST00000377100.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.76A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.123A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.76A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.180A>G
  hgvsp: ENST00000377059.3:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln60Gln
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

10-21827793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827793
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827793
    reference: chr 10
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.192A>G
  hgvsp: ENST00000377091.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.88A>G
  hgvsp: ENST00000430455.1:c.88A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.192A>G
  hgvsp: ENST00000446906.2:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.88A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.223A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.192A>G
  hgvsp: ENST00000377100.3:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.135A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.192A>G
  hgvsp: ENST00000377072.3:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.88A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.192A>G
  hgvsp: ENST00000307729.7:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.192A>G
  hgvsp: ENST00000377059.3:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4060A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.219A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly64Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

10-21827796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827796
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827796
    reference: chr 10
allele count: 37849
allele frequency: 3.118275140470266e-1
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.195G>A
  hgvsp: ENST00000446906.2:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.91G>A
  hgvsp: ENST00000430455.1:c.91G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.91G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.195G>A
  hgvsp: ENST00000377059.3:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.195G>A
  hgvsp: ENST00000377100.3:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.195G>A
  hgvsp: ENST00000377091.2:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.195G>A
  hgvsp: ENST00000307729.7:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4063G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.195G>A
  hgvsp: ENST00000377072.3:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.138G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.226G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.222G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.91G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 1806
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.25e1
  variant carriers: 677
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 9.25e1
  variant carriers: 1850
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 2.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 986
genotype depth: GenotypeDepth
  all individuals: 12629
  bin: 9.75e1
  variant carriers: 12129
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 5.75e1
  variant carriers: 1567
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 8.25e1
  variant carriers: 2114
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 221
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 7.25e1
  variant carriers: 2069
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.75e1
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 7.75e1
  variant carriers: 2090
genotype quality: GenotypeQuality
hgvs: p.Pro65Pro
num of homozygotes: 6629
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

10-21827796-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827796
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827796
    reference: chr 10
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.91G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.138G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.195G>T
  hgvsp: ENST00000377091.2:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.91G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.195G>T
  hgvsp: ENST00000446906.2:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.222G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.226G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.195G>T
  hgvsp: ENST00000377100.3:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.91G>T
  hgvsp: ENST00000430455.1:c.91G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.195G>T
  hgvsp: ENST00000377059.3:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.195G>T
  hgvsp: ENST00000307729.7:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4063G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.195G>T
  hgvsp: ENST00000377072.3:c.195G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro65Pro
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

10-21827826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827826
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827826
    reference: chr 10
allele count: 3
allele frequency: 2.472717681579902e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.121G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.168G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.252G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.256G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.225G>A
  hgvsp: ENST00000377100.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.121G>A
  hgvsp: ENST00000430455.1:c.121G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.225G>A
  hgvsp: ENST00000446906.2:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.225G>A
  hgvsp: ENST00000377091.2:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4093G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.225G>A
  hgvsp: ENST00000377059.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.225G>A
  hgvsp: ENST00000377072.3:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.225G>A
  hgvsp: ENST00000307729.7:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.121G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu75Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

10-21827856-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827856
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827856
    reference: chr 10
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4123T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.282T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+15T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+15T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-21827857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827857
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827857
    reference: chr 10
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4124C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.283C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+16C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

10-21827863-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827863
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827863
    reference: chr 10
allele count: 4
allele frequency: 3.318510652419194e-5
allele num: 120536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4130C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.289C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+22C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+22C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

10-21827870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827870
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827870
    reference: chr 10
allele count: 4
allele frequency: 3.325241911349051e-5
allele num: 120292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4137C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.296C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+29C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+29C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

10-21827873-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827873
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827873
    reference: chr 10
allele count: 3
allele frequency: 2.494180246092451e-5
allele num: 120280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.299T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4140T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+32T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18548
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

10-21827884-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21827884
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21827884
    reference: chr 10
allele count: 1
allele frequency: 8.38841727342885e-6
allele num: 119212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000471315
  gene symbol: MLLT10
  hgvsc: ENST00000471315.1:n.310T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.271+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+4151T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.136+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.240+43T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+43T>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14919
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

10-21840697-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840697
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840697
    reference: chr 10
allele count: 37
allele frequency: 4.192159528665307e-3
allele num: 8826
alternate allele: A
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 5
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 166
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 1.388888888888889e-2
  allele num: 72
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 35
  allele frequency: 5.634256278171281e-3
  allele num: 6212
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-21840697-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840697
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840698
    reference: chr 10
allele count: 1
allele frequency: 1.133016088828461e-4
allele num: 8826
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4872dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16967dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12859dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5850dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-45dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10410dupA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12859dupA
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

10-21840697-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840697
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840696
    reference: chr 10
allele count: 8
allele frequency: 9.064128710627691e-4
allele num: 8826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4872delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5850delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12859delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10410delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-45delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16967delA
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12859delA
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: TA
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

10-21840698-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840698
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840698
    reference: chr 10
allele count: 11
allele frequency: 1.185089420383538e-3
allele num: 9282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-47A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5852A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16965A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10408A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4874A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12857A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12857A>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

10-21840703-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840703
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840703
    reference: chr 10
allele count: 1
allele frequency: 9.958175662218681e-5
allele num: 10042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10413A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4869A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16970A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5847A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12862A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-42A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12862A>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

10-21840717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840717
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840717
    reference: chr 10
allele count: 2
allele frequency: 1.958096729978461e-4
allele num: 10214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-28C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16984C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10427C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4855C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12876C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5833C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12876C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

10-21840723-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840723
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840723
    reference: chr 10
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5827C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10433C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-22C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4849C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12882C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+16990C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12882C>G
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

10-21840729-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840729
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840730
    reference: chr 10
allele count: 760
allele frequency: 1.300924340979117e-1
allele num: 5842
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-3dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10452dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5808dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4830dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17009dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12901dupT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12901dupT
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 374
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

10-21840729-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840729
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840731
    reference: chr 10
allele count: 24
allele frequency: 4.108182129407737e-3
allele num: 5842
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5809_272-5808dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12900_183+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10451_235+10452dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17008_56+17009dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-4_241-3dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12900_240+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12900_136+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12900_240+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12900_240+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12900_136+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4831_241-4830dupTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12900_240+12901dupTT
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-21840729-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840729
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840728
    reference: chr 10
allele count: 1906
allele frequency: 3.262581307771311e-1
allele num: 5842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17009delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10452delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4830delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5808delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12901delT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-3delT
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 599
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 760
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.75e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: CT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

10-21840729-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840729
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840727
    reference: chr 10
allele count: 82
allele frequency: 1.40362889421431e-2
allele num: 5842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.241-4_241-3delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17008_56+17009delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12900_240+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12900_240+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12900_240+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12900_136+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10451_235+10452delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12900_136+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12900_240+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4831_241-4830delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12900_183+12901delTT
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5809_272-5808delTT
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: CTT
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-21840755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840755
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840755
    reference: chr 10
allele count: 1
allele frequency: 1.023960679909891e-4
allele num: 9766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10465G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.251G>A
  hgvsp: ENSP00000366295.2:p.Arg84His
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4817G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17022G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5795G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12914G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12914G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg84His
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

10-21840765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840765
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840765
    reference: chr 10
allele count: 1
allele frequency: 1.051967178624027e-4
allele num: 9506
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5785C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4807C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10475C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.261C>T
  hgvsp: ENST00000377091.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17032C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12924C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12924C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala87Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

10-21840772-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840772
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840772
    reference: chr 10
allele count: 1
allele frequency: 1.130198915009042e-4
allele num: 8848
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17039A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4800A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10482A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12931A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.268A>G
  hgvsp: ENSP00000366295.2:p.Lys90Glu
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5778A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12931A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys90Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

10-21840773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840773
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840773
    reference: chr 10
allele count: 1
allele frequency: 1.134301270417423e-4
allele num: 8816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17040A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10483A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5777A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4799A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.269A>G
  hgvsp: ENSP00000366295.2:p.Lys90Arg
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12932A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12932A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys90Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-21840809-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840809
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840809
    reference: chr 10
allele count: 1
allele frequency: 1.544163063619518e-4
allele num: 6476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.305T>C
  hgvsp: ENSP00000366295.2:p.Leu102Pro
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17076T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10519T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4763T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5741T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12968T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12968T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-21840811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840811
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840811
    reference: chr 10
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4761C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10521C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17078C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.307C>T
  hgvsp: ENSP00000366295.2:p.Leu103Phe
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12970C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5739C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu103Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

10-21840816-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840816
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840816
    reference: chr 10
allele count: 32
allele frequency: 5.616005616005616e-3
allele num: 5698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10526C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17083C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.312C>T
  hgvsp: ENST00000377091.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12975C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5734C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4756C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro104Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

10-21840827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840827
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840827
    reference: chr 10
allele count: 1
allele frequency: 2.145922746781116e-4
allele num: 4660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4745G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.323G>A
  hgvsp: ENSP00000366295.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17094G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10537G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5723G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+12986G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+12986G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg108Gln
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

10-21840886-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21840886
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21840886
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+17153G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-5664G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-4686G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+10596G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.346+36G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.136+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+13045G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+13045G>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-21845523-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845523
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845523
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 40586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21790T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-49T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15233T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17682T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17682T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-49T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15381T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17682T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1027T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17682T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17682T>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17682T>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28444
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

10-21845526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845526
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845526
    reference: chr 10
allele count: 1
allele frequency: 2.473533194815474e-5
allele num: 40428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1024C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15378C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17685C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-46C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17685C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17685C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-46C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17685C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21793C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15236C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17685C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17685C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13868
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28457
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

10-21845527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845527
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845527
    reference: chr 10
allele count: 2
allele frequency: 4.895721139723881e-5
allele num: 40852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15237G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-45G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15377G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21794G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17686G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17686G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-45G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17686G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17686G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1023G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17686G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17686G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28626
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13905
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

10-21845528-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845528
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845528
    reference: chr 10
allele count: 5
allele frequency: 1.22327151734599e-4
allele num: 40874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1022C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15376C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15238C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21795C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17687C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-44C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-44C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13899
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28798
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-21845532-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845532
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845532
    reference: chr 10
allele count: 1
allele frequency: 2.384244909637118e-5
allele num: 41942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1018A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15242A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15372A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21799A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-40A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17691A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-40A>C
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29900
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

10-21845535-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845535
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845535
    reference: chr 10
allele count: 1
allele frequency: 2.327313349469373e-5
allele num: 42968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-37A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15245A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1015A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15369A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17694A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-37A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13469
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30403
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

10-21845546-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845546
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845546
    reference: chr 10
allele count: 14
allele frequency: 2.923854475585815e-4
allele num: 47882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-1004A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241-26A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21813A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15358A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347-26A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17705A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15256A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30664
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

10-21845549-GGATTGTTTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845549
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845540
    reference: chr 10
allele count: 1
allele frequency: 1.999680051191809e-5
allele num: 50008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  variant of: http://identifiers.org/hgnc/16063
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: GGATTGTTTT
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

10-21845572-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845572
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845572
    reference: chr 10
allele count: 1
allele frequency: 1.290089532213536e-5
allele num: 77514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.347A>G
  hgvsp: ENSP00000366295.2:p.Asn116Ser
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-978A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15332A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21839A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17731A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15282A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.241A>G
  hgvsp: ENSP00000366304.3:p.Met81Val
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27548
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met81Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

10-21845587-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845587
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845587
    reference: chr 10
allele count: 2
allele frequency: 2.140731702095776e-5
allele num: 93426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21854T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17746T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15297T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17746T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17746T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17746T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.256T>C
  hgvsp: ENSP00000366304.3:p.Cys86Arg
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15317T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.362T>C
  hgvsp: ENSP00000366295.2:p.Leu121Pro
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-963T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17746T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17746T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36276
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys86Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

10-21845591-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845591
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845591
    reference: chr 10
allele count: 2
allele frequency: 2.071508472469652e-5
allele num: 96548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.366G>A
  hgvsp: ENST00000377091.2:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.260G>A
  hgvsp: ENSP00000366304.3:p.Trp87Ter
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15313G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-959G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17750G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21858G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15301G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37861
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp87Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

10-21845593-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845593
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845593
    reference: chr 10
allele count: 1
allele frequency: 1.025136343133637e-5
allele num: 97548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15311T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15303T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17752T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-957T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17752T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17752T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.262T>C
  hgvsp: ENST00000377100.3:c.262T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17752T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17752T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.368T>C
  hgvsp: ENSP00000366295.2:p.Val123Ala
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21860T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17752T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38238
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val123Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-21845598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845598
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845598
    reference: chr 10
allele count: 55
allele frequency: 5.5178779244753e-4
allele num: 99676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.373C>T
  hgvsp: ENSP00000366295.2:p.Leu125Phe
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.267C>T
  hgvsp: ENST00000377100.3:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21865C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-952C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15308C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17757C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15306C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38782
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu125Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

10-21845598-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845598
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845598
    reference: chr 10
allele count: 4
allele frequency: 4.013002126891127e-5
allele num: 99676
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15308C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.373C>G
  hgvsp: ENSP00000366295.2:p.Leu125Val
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21865C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-952C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.267C>G
  hgvsp: ENST00000377100.3:c.267C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17757C>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15306C>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38782
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu125Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

10-21845610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845610
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845610
    reference: chr 10
allele count: 5
allele frequency: 4.830824525129949e-5
allele num: 103502
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17769C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.279C>T
  hgvsp: ENST00000377100.3:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17769C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17769C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21877C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-940C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15294C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17769C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*4C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17769C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15320C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17769C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40228
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn93Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

10-21845611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845611
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845611
    reference: chr 10
allele count: 1
allele frequency: 9.654932705119045e-6
allele num: 103574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21878G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*5G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.280G>A
  hgvsp: ENSP00000366304.3:p.Val94Ile
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17770G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15321G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-939G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15293G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val94Ile
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

10-21845618-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845618
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845618
    reference: chr 10
allele count: 1
allele frequency: 9.557122923715046e-6
allele num: 104634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17777C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17777C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15286C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-932C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.287C>T
  hgvsp: ENSP00000366304.3:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17777C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21885C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15328C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17777C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*12C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17777C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17777C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-21845621-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845621
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845621
    reference: chr 10
allele count: 1
allele frequency: 9.530526275660943e-6
allele num: 104926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17780G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-929G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17780G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17780G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.290G>T
  hgvsp: ENSP00000366304.3:p.Gly97Val
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*15G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15331G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17780G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15283G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17780G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21888G>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17780G>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly97Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/10-21845624-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845624
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845624
    reference: chr 10
allele count: 1
allele frequency: 9.522721212813774e-6
allele num: 105012
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17783A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*18A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15280A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17783A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-926A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21891A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17783A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17783A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17783A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.293A>C
  hgvsp: ENSP00000366304.3:p.Tyr98Ser
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15334A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17783A>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr98Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

10-21845624-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845624
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845624
    reference: chr 10
allele count: 1
allele frequency: 9.522721212813774e-6
allele num: 105012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17783A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17783A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15280A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15334A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17783A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*18A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17783A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-926A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21891A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.293A>G
  hgvsp: ENSP00000366304.3:p.Tyr98Cys
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17783A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17783A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7551
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr98Cys
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: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

10-21845627-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845627
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845627
    reference: chr 10
allele count: 1
allele frequency: 9.512213682368161e-6
allele num: 105128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17786T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17786T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17786T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17786T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17786T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*21T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15337T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21894T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15277T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.296T>C
  hgvsp: ENSP00000366304.3:p.Ile99Thr
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-923T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17786T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40013
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile99Thr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-21845628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845628
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845628
    reference: chr 10
allele count: 3
allele frequency: 2.854913305799281e-5
allele num: 105082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17787A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17787A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*22A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.297A>G
  hgvsp: ENSP00000366304.3:p.Ile99Met
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-922A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17787A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17787A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15338A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17787A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15276A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21895A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17787A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39924
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile99Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-21845633-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845633
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845633
    reference: chr 10
allele count: 1
allele frequency: 9.596560592683583e-6
allele num: 104204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-917A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15271A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17792A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17792A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17792A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.302A>C
  hgvsp: ENSP00000366304.3:p.His101Pro
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*27A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17792A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21900A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15343A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17792A>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17792A>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38526
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His101Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

10-21845640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845640
    reference: chr 10
allele count: 3
allele frequency: 2.902083696093795e-5
allele num: 103374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17799C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17799C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17799C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15264C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17799C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17799C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21907C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-910C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15350C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.309C>T
  hgvsp: ENST00000377100.3:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17799C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys103Cys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-21845641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845641
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845641
    reference: chr 10
allele count: 3
allele frequency: 2.908949869097256e-5
allele num: 103130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17800G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17800G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-909G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21908G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17800G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17800G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15263G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17800G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*35G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.310G>A
  hgvsp: ENSP00000366304.3:p.Ala104Thr
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15351G>A
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17800G>A
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8039
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37028
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala104Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

10-21845643-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845643
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845643
    reference: chr 10
allele count: 1
allele frequency: 9.725545116803797e-6
allele num: 102822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15261A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*37A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.312A>G
  hgvsp: ENST00000377100.3:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15353A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-907A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17802A>G
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21910A>G
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala104Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

10-21845644-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845644
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845644
    reference: chr 10
allele count: 1
allele frequency: 9.747728779194448e-6
allele num: 102588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.313T>C
  hgvsp: ENSP00000366304.3:p.Cys105Arg
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*38T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-906T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21911T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15260T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17803T>C
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15354T>C
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys105Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

10-21845649-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845649
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845649
    reference: chr 10
allele count: 1
allele frequency: 9.890218573830481e-6
allele num: 101110
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17808A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17808A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.318A>T
  hgvsp: ENST00000377100.3:c.318A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15255A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17808A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15359A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21916A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17808A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-901A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*43A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17808A>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17808A>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala106Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

10-21845658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 21845658
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 21845658
    reference: chr 10
allele count: 5
allele frequency: 5.191029900332226e-5
allele num: 96320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000479634
  gene symbol: MLLT10
  hgvsc: ENST00000479634.1:n.56+21925C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366272
  ensembl transcript: ENST00000377072
  gene symbol: MLLT10
  hgvsc: ENST00000377072.3:c.240+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000476557
  gene symbol: MLLT10
  hgvsc: ENST00000476557.1:n.183+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000495130
  gene symbol: MLLT10
  hgvsc: ENST00000495130.1:n.272-892C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000401406
  ensembl transcript: ENST00000446906
  gene symbol: MLLT10
  hgvsc: ENST00000446906.2:c.240+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366295
  ensembl transcript: ENST00000377091
  gene symbol: MLLT10
  hgvsc: ENST00000377091.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000397800
  ensembl transcript: ENST00000430455
  gene symbol: MLLT10
  hgvsc: ENST00000430455.1:c.136+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366258
  ensembl transcript: ENST00000377059
  gene symbol: MLLT10
  hgvsc: ENST00000377059.3:c.240+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000307411
  ensembl transcript: ENST00000307729
  gene symbol: MLLT10
  hgvsc: ENST00000307729.7:c.240+17817C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000078403
  ensembl protein: ENSP00000366304
  ensembl transcript: ENST00000377100
  gene symbol: MLLT10
  hgvsc: ENST00000377100.3:c.327C>T
  hgvsp: ENST00000377100.3:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000462999
  gene symbol: MLLT10
  hgvsc: ENST00000462999.1:n.235+15368C>T
  variant of: http://identifiers.org/hgnc/16063
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000078403
  ensembl transcript: ENST00000480415
  gene symbol: MLLT10
  hgvsc: ENST00000480415.1:n.137-15246C>T
  variant of: http://identifiers.org/hgnc/16063
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29975
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His109His
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8568
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20390
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521745746720638e-5
allele num: 65714
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.774187e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.195e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 821
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6941
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3734
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8579
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2182
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.215040397762585e-5
allele num: 16090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65760
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.195e1

MQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.791668e6

GenotypeDepth
all individuals: 125
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8591
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24546
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7058
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65788
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: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.810863e6

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 2.365e0

MQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.298e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 610
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1369
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 691
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8618
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 25608
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.911597887737141e-4
allele num: 10226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.588e0

DP
type: SiteQuality
SIO_000300: 1.821593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

GenotypeDepth
all individuals: 125
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 657
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.169792694965449e-5
allele num: 16208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.675e0

FS
type: SiteQuality
SIO_000300: 1.4062e1

VQSLOD
type: SiteQuality
SIO_000300: -1.801e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

DP
type: SiteQuality
SIO_000300: 1.842999e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeDepth
all individuals: 482
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1369
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3006
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8721
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29776
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
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: 11556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

FS
type: SiteQuality
SIO_000300: 8.318e0

MQRankSum
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SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e-1

QD
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SIO_000300: 1.18e1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.878235e6

ClippingRankSum
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SIO_000300: -4.1e-2

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -3.91e0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
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
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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DP
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MQ
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SIO_000300: 5.951e1

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.996821684507211e-5
allele num: 66702
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

FS
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
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SIO_000300: 1.5e-2

BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.2e-2

VQSLOD
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SIO_000300: 2.53e0

QD
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SIO_000300: 1.477e1

ReadPosRankSum
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SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 1.886969e6

GenotypeDepth
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
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

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
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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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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SIO_000300: -3.32e-1

ClippingRankSum
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SIO_000300: 6.879999999999999e-1

FS
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SIO_000300: 8.24e-1

BaseQRankSum
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SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.850000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.888028e6

QD
type: SiteQuality
SIO_000300: 1.22e1

GenotypeDepth
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variant carriers: 1930

GenotypeDepth
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variant carriers: 1251

GenotypeDepth
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variant carriers: 11

GenotypeDepth
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variant carriers: 1982

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 31135

GenotypeQuality
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variant carriers: 23

European (Non-Finnish)
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allele count: 24362
allele frequency: 3.651378896882494e-1
allele num: 66720
num of homozygotes: 4524

South Asian
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allele count: 4192
allele frequency: 2.538759689922481e-1
allele num: 16512
num of homozygotes: 560

Latino
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allele count: 2256
allele frequency: 1.949196474857439e-1
allele num: 11574
num of homozygotes: 260

East Asian
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allele count: 383
allele frequency: 4.42876965772433e-2
allele num: 8648
num of homozygotes: 9

European (Finnish)
type: Population
allele count: 2168
allele frequency: 3.277895373450257e-1
allele num: 6614
num of homozygotes: 375

Other
type: Population
allele count: 303
allele frequency: 3.337004405286343e-1
allele num: 908
num of homozygotes: 49

African
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allele count: 4185
allele frequency: 4.023264756777543e-1
allele num: 10402
num of homozygotes: 852

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

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

African
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
type: Population
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BaseQRankSum
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SIO_000300: 1.49e-1

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

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

European (Non-Finnish)
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East Asian
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Latino
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allele num: 11566
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South Asian
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African
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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FS
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DP
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 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: 0.0e0
allele num: 66320
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele num: 10372
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East Asian
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 66190
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11518
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6600
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African
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East Asian
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allele num: 8606
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Other
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DP
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

African
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allele count: 3
allele frequency: 2.903038513644281e-4
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 1.86e-1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

Latino
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allele num: 11504
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East Asian
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allele frequency: 0.0e0
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African
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South Asian
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allele num: 16334
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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African
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Latino
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QD
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MQRankSum
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VQSLOD
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DP
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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European (Non-Finnish)
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East Asian
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Other
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FS
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VQSLOD
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
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Other
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Latino
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European (Non-Finnish)
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African
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South Asian
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East Asian
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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VQSLOD
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FS
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DP
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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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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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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East Asian
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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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FS
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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FS
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QD
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African
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European (Finnish)
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East Asian
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Latino
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FS
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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African
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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MQ
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VQSLOD
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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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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South Asian
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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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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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East Asian
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European (Finnish)
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South Asian
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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MQ
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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VQSLOD
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MQ
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BaseQRankSum
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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African
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East Asian
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Latino
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Non-Finnish)
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allele frequency: 1.308139534883721e-2
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East Asian
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African
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European (Finnish)
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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DP
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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MQ
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QD
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DP
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 2546
num of homozygotes: 0

African
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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South Asian
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East Asian
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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MQRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 0.0e0

GenotypeDepth
all individuals: 13720
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2516
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 2.5e0
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5420
bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.491620111731844e-4
allele num: 2864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7144
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.19829e5

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

QD
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SIO_000300: 9.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 4402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.260395364689843e-5
allele num: 23472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.271e1

DP
type: SiteQuality
SIO_000300: 6.35465e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.133e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

GenotypeDepth
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 481
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 1

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 9106
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variant carriers: 0

GenotypeQuality
all individuals: 886
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28957
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variant carriers: 0

GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 3.094059405940594e-4
allele num: 3232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.594700686947988e-3
allele num: 8152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

DP
type: SiteQuality
SIO_000300: 7.08729e5

GenotypeQuality
all individuals: 4472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
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variant carriers: 0

GenotypeQuality
all individuals: 4670
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variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1927
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variant carriers: 0

GenotypeQuality
all individuals: 10388
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variant carriers: 0

GenotypeQuality
all individuals: 325
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GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 483
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variant carriers: 0

GenotypeQuality
all individuals: 28523
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GenotypeQuality
all individuals: 914
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 1091
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variant carriers: 1

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.699866804795027e-5
allele num: 27028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3424
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.088e-1

QD
type: SiteQuality
SIO_000300: 2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 7.34242e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

FS
type: SiteQuality
SIO_000300: 2.343e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

GenotypeDepth
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 1094
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variant carriers: 1

GenotypeQuality
all individuals: 259
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variant carriers: 0

GenotypeQuality
all individuals: 2049
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variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 27765
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 482
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 422
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GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 710
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GenotypeQuality
all individuals: 185
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GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 726
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GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4312
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.651800462504129e-4
allele num: 6054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.429999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.409e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 2.197e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

DP
type: SiteQuality
SIO_000300: 9.99125e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

GenotypeDepth
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
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variant carriers: 0

GenotypeQuality
all individuals: 132
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 1067
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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
all individuals: 279
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 1096
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6818
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.686727565824826e-4
allele num: 7444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12698
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 9.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 1.147259e6

QD
type: SiteQuality
SIO_000300: 1.317e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

GenotypeDepth
all individuals: 205
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.5e0
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GenotypeQuality
all individuals: 285
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variant carriers: 0

GenotypeQuality
all individuals: 9536
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 875
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 883
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 381
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GenotypeQuality
all individuals: 100
bin: 1.75e1
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GenotypeQuality
all individuals: 1882
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GenotypeQuality
all individuals: 134
bin: 8.25e1
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GenotypeQuality
all individuals: 39870
bin: 6.25e1
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GenotypeQuality
all individuals: 1096
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 364
bin: 7.25e1
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GenotypeQuality
all individuals: 277
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5478
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.176278563656148e-4
allele num: 9190
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

DP
type: SiteQuality
SIO_000300: 1.178366e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

FS
type: SiteQuality
SIO_000300: 3.022e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.143e0

GenotypeDepth
all individuals: 2235
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 830
bin: 2.75e1
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 385
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 1095
bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 1934
bin: 6.75e1
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GenotypeQuality
all individuals: 569
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.606876616461281e-5
allele num: 13146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

DP
type: SiteQuality
SIO_000300: 1.186628e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
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SIO_000300: -1.424e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

GenotypeDepth
all individuals: 79
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 9.75e1
variant carriers: 56

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 40944
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 1994
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.582278481012658e-3
allele num: 5688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 45
allele frequency: 8.143027758676848e-4
allele num: 55262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.388888888888889e-4
allele num: 7200
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.082e1

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

DP
type: SiteQuality
SIO_000300: 1.212507e6

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

GenotypeDepth
all individuals: 97
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1154
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1994
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variant carriers: 0

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55262
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.166666666666667e-4
allele num: 7200
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.277465508431272e-4
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

DP
type: SiteQuality
SIO_000300: 1.212507e6

GenotypeDepth
all individuals: 85
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 43716
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 489
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6326
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variant carriers: 0

GenotypeQuality
all individuals: 359
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GenotypeQuality
all individuals: 780
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variant carriers: 1

GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 2138
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GenotypeQuality
all individuals: 1100
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 407
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.707767328456984e-5
allele num: 57420
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.249759e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

QD
type: SiteQuality
SIO_000300: 6.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.976e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

GenotypeDepth
all individuals: 65
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
all individuals: 506
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 6337
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variant carriers: 0

GenotypeQuality
all individuals: 61
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1096
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 43204
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.348072256672958e-4
allele num: 7418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8010
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.250489e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -1.041e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
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SIO_000300: 4.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: -2.715e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 461
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variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.722415515518964e-5
allele num: 58058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.261229e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.376e0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 492
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GenotypeQuality
all individuals: 2227
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variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 321
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8084
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.334400854016547e-4
allele num: 7494
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.842e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 9.389999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.265e-1

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.115e1

DP
type: SiteQuality
SIO_000300: 1.264622e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 158
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GenotypeQuality
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GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 142
bin: 8.25e1
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GenotypeQuality
all individuals: 452
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GenotypeQuality
all individuals: 1097
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GenotypeQuality
all individuals: 5970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 6.75e1
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GenotypeQuality
all individuals: 343
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.71650245459851e-5
allele num: 58258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14090
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 1.26363e6

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.989e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
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SIO_000300: 1.44e0

InbreedingCoeff
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SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.39e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.71650245459851e-5
allele num: 58258
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 1.989e0

VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.26363e6

ClippingRankSum
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SIO_000300: 1.44e0

InbreedingCoeff
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SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.714266122672884e-5
allele num: 58334
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

VQSLOD
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SIO_000300: -1.713e0

ReadPosRankSum
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SIO_000300: -3.9e-2

DP
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SIO_000300: 1.264876e6

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -1.8e-3

MQRankSum
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SIO_000300: -1.273e0

MQ
type: SiteQuality
SIO_000300: 5.788e1

QD
type: SiteQuality
SIO_000300: 1.349e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.56e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14114
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.144915108900703e-5
allele num: 58310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

DP
type: SiteQuality
SIO_000300: 1.264392e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 140
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.730283420424266e-5
allele num: 57794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

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

African
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.154e0

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
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SIO_000300: 9.56e-1

DP
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SIO_000300: 1.253179e6

FS
type: SiteQuality
SIO_000300: 1.603e0

ClippingRankSum
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SIO_000300: 9.56e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 9.81e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1098
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 3
allele frequency: 2.987452698665605e-4
allele num: 10042
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13878
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6020
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.356e1

MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.9e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

DP
type: SiteQuality
SIO_000300: 1.245181e6

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7362
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.246222719641858e-5
allele num: 57184
num of homozygotes: 0

Other
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VQSLOD
type: SiteQuality
SIO_000300: -7.924e-1

DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.753401599102258e-5
allele num: 57032
num of homozygotes: 0

African
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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
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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ClippingRankSum
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SIO_000300: -1.485e0

QD
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SIO_000300: 1.328e1

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

FS
type: SiteQuality
SIO_000300: 1.494e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.864e0

DP
type: SiteQuality
SIO_000300: 1.236479e6

GenotypeDepth
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 607
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41465
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8544
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.757716374885749e-5
allele num: 56892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.375e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

FS
type: SiteQuality
SIO_000300: 1.603e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.193e0

DP
type: SiteQuality
SIO_000300: 1.233083e6

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9858
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.783739431343869e-5
allele num: 56062
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.551e0

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

DP
type: SiteQuality
SIO_000300: 1.21459e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeDepth
all individuals: 48
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 974
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13806
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 949
bin: 7.5e0
variant carriers: 0