19-1356315-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356315
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356315
    reference: chr 19
allele count: 1
allele frequency: 1.131196126784462e-5
allele num: 88402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-693C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-69-5C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-66-8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.100-8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-66-8C>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23881
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2946
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 2.75e1
  variant carriers: 0
hgvs: c.-69-5C>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

19-1356316-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356316
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356316
    reference: chr 19
allele count: 7
allele frequency: 7.70568679685608e-5
allele num: 90842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-66-7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-692G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.100-7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-69-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-66-7G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25630
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14854
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3836
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 26449
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 0
hgvs: c.-69-4G>A
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

19-1356319-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356319
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356319
    reference: chr 19
allele count: 1
allele frequency: 1.051701653274999e-5
allele num: 95084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-66-4C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-66-4C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.100-4C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-689C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-69-1C>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12933
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 7.25e1
  variant carriers: 0
hgvs: c.-69-1C>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/19-1356325-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356325
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356324
    reference: chr 19
allele count: 1
allele frequency: 9.78320419503796e-6
allele num: 102216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-682delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.103delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-383delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-63delA
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: CA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

19-1356326-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356326
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356326
    reference: chr 19
allele count: 1
allele frequency: 9.646364285300871e-6
allele num: 103666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-682A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-383A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.103A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-1356328-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356328
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356328
    reference: chr 19
allele count: 555
allele frequency: 5.239902566136067e-3
allele num: 105918
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-381A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-680A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.105A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-61A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7596
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 33843
  bin: 2.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 2.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 9.75e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 4138
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4299
  bin: 9.75e1
  variant carriers: 533
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 14
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

19-1356329-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356329
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356329
    reference: chr 19
allele count: 1
allele frequency: 9.394611250986435e-6
allele num: 106444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-380T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.106T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-679T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-60T>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

19-1356330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356330
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356330
    reference: chr 19
allele count: 3
allele frequency: 2.79647271574787e-5
allele num: 107278
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-379T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-678T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.107T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34583
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-1356331-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356331
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356332
    reference: chr 19
allele count: 1
allele frequency: 9.261660430481977e-6
allele num: 107972
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.108_109insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-378_-377insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-677_43-676insT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-58_-57insT
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6751
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

19-1356340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356340
    reference: chr 19
allele count: 1
allele frequency: 8.7415643903633e-6
allele num: 114396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.117C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-369C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-668C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

19-1356342-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356342
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356341
    reference: chr 19
allele count: 5
allele frequency: 4.324212128550178e-5
allele num: 115628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-364delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.122delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-663delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-44delG
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37947
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3919
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: TG
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

19-1356345-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356345
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356345
    reference: chr 19
allele count: 1
allele frequency: 8.564283512041383e-6
allele num: 116764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-364G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-663G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.122G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-44G>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4893
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-1356350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356350
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356350
    reference: chr 19
allele count: 1
allele frequency: 8.469121582709441e-6
allele num: 118076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.127C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-359C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-658C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5005
  bin: 6.75e1
  variant carriers: 0
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: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-1356365-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356365
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356365
    reference: chr 19
allele count: 2
allele frequency: 1.6619025460347e-5
allele num: 120344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-643T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.142T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-344T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-24T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-1356370-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356370
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356370
    reference: chr 19
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-339A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-638A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.147A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-19A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

19-1356374-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356374
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356374
    reference: chr 19
allele count: 1
allele frequency: 8.27841981522567e-6
allele num: 120796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-335G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-15G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.151G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-634G>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

19-1356383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356383
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356383
    reference: chr 19
allele count: 3
allele frequency: 2.479707725116133e-5
allele num: 120982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-625G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.160G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-326G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

19-1356384-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356384
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356384
    reference: chr 19
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-325T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-624T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.161T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-5T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-1356385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356385
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356385
    reference: chr 19
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-324G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.162G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-623G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-4G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-1356386-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356386
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356386
    reference: chr 19
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-622T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-323T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.-3T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.163T>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

19-1356391-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356391
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356391
    reference: chr 19
allele count: 4
allele frequency: 3.30398295144797e-5
allele num: 121066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.3G>A
  hgvsp: ENSP00000466891.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-617G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.3G>A
  hgvsp: ENSP00000468557.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.3G>A
  hgvsp: ENSP00000467287.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.3G>A
  hgvsp: ENSP00000467083.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.168G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.3G>A
  hgvsp: ENSP00000465838.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-318G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.3G>A
  hgvsp: ENSP00000345789.3:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.3G>A
  hgvsp: ENSP00000468322.1:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.3G>A
  hgvsp: ENSP00000394925.2:p.Met1?
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

19-1356403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356403
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356403
    reference: chr 19
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.180C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.15C>T
  hgvsp: ENST00000591337.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.15C>T
  hgvsp: ENST00000592374.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-306C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.15C>T
  hgvsp: ENST00000591806.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.15C>T
  hgvsp: ENST00000587460.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.15C>T
  hgvsp: ENST00000591433.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-605C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.15C>T
  hgvsp: ENST00000415183.3:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.15C>T
  hgvsp: ENST00000588810.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.15C>T
  hgvsp: ENST00000344663.3:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala5Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

19-1356406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356406
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356406
    reference: chr 19
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.18G>A
  hgvsp: ENST00000587460.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.18G>A
  hgvsp: ENST00000592374.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.18G>A
  hgvsp: ENST00000591433.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.18G>A
  hgvsp: ENST00000591806.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.18G>A
  hgvsp: ENST00000588810.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.183G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.18G>A
  hgvsp: ENST00000591337.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.18G>A
  hgvsp: ENST00000344663.3:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-602G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.18G>A
  hgvsp: ENST00000415183.3:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-303G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys6Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

19-1356407-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356407
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356407
    reference: chr 19
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.19T>C
  hgvsp: ENSP00000468557.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.19T>C
  hgvsp: ENSP00000345789.3:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.19T>C
  hgvsp: ENSP00000394925.2:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-601T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.184T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.19T>C
  hgvsp: ENSP00000465838.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.19T>C
  hgvsp: ENSP00000466891.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.19T>C
  hgvsp: ENSP00000467287.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.19T>C
  hgvsp: ENSP00000468322.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-302T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.19T>C
  hgvsp: ENSP00000467083.1:p.Tyr7His
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr7His
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

19-1356410-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356410
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356410
    reference: chr 19
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.22G>A
  hgvsp: ENSP00000345789.3:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.22G>A
  hgvsp: ENSP00000467287.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.22G>A
  hgvsp: ENSP00000394925.2:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-299G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.22G>A
  hgvsp: ENSP00000468322.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.22G>A
  hgvsp: ENSP00000468557.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.22G>A
  hgvsp: ENSP00000466891.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.22G>A
  hgvsp: ENSP00000465838.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.187G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-598G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.22G>A
  hgvsp: ENSP00000467083.1:p.Val8Ile
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val8Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-1356419-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356419
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356419
    reference: chr 19
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.31C>G
  hgvsp: ENSP00000345789.3:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.31C>G
  hgvsp: ENSP00000468557.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.31C>G
  hgvsp: ENSP00000465838.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-589C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.31C>G
  hgvsp: ENSP00000467287.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.31C>G
  hgvsp: ENSP00000468322.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.196C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.31C>G
  hgvsp: ENSP00000466891.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.31C>G
  hgvsp: ENSP00000467083.1:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-290C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.31C>G
  hgvsp: ENSP00000394925.2:p.Arg11Gly
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-1356421-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356421
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356421
    reference: chr 19
allele count: 3
allele frequency: 2.474920802534319e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.33A>C
  hgvsp: ENST00000344663.3:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.33A>C
  hgvsp: ENST00000592374.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.33A>C
  hgvsp: ENST00000588810.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.33A>C
  hgvsp: ENST00000587460.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.198A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.33A>C
  hgvsp: ENST00000591433.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.33A>C
  hgvsp: ENST00000591806.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.33A>C
  hgvsp: ENST00000591337.1:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.33A>C
  hgvsp: ENST00000415183.3:c.33A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-288A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-587A>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

19-1356445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356445
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356445
    reference: chr 19
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.57G>A
  hgvsp: ENST00000587460.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.57G>A
  hgvsp: ENST00000591433.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.222G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-264G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.57G>A
  hgvsp: ENST00000415183.3:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.57G>A
  hgvsp: ENST00000588810.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.57G>A
  hgvsp: ENST00000592374.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.57G>A
  hgvsp: ENST00000591337.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.57G>A
  hgvsp: ENST00000591806.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.57G>A
  hgvsp: ENST00000344663.3:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-563G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala19Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-1356452-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356452
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356452
    reference: chr 19
allele count: 61
allele frequency: 5.135977098593922e-4
allele num: 118770
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-556A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+4A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+4A>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37671
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.60+4A>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

19-1356455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356455
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356455
    reference: chr 19
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+7G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-553G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+7G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 37337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.60+7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

19-1356456-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356456
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356456
    reference: chr 19
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-552C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+8C>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.60+8C>G
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

19-1356457-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356457
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356457
    reference: chr 19
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-551C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+9C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

19-1356460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356460
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356460
    reference: chr 19
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-548T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+12T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-1356473-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356473
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356473
    reference: chr 19
allele count: 4
allele frequency: 3.309778741291145e-5
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-535C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+25C>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36017
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

19-1356476-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356476
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356476
    reference: chr 19
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+28G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-532G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+28G>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

19-1356478-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356478
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356478
    reference: chr 19
allele count: 2
allele frequency: 1.655492095025246e-5
allele num: 120810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-530C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+30C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35143
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

19-1356485-A-ATC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356485
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356487
    reference: chr 19
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
alternate allele: ATC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-522_43-521insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+38_-261+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+38_225+39insCT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+38_60+39insCT
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

19-1356485-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356485
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356485
    reference: chr 19
allele count: 14
allele frequency: 1.159439493821844e-4
allele num: 120748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-523A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+37A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32135
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

19-1356495-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356495
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356495
    reference: chr 19
allele count: 58
allele frequency: 4.826013878950259e-4
allele num: 120182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-261+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.225+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-513G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.60+47G>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30715
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

19-1356961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356961
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356961
    reference: chr 19
allele count: 1
allele frequency: 8.851594172110397e-6
allele num: 112974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-47C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3491
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-1356981-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356981
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356981
    reference: chr 19
allele count: 59
allele frequency: 5.132130617073468e-4
allele num: 114962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.5A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-27A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29350
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

19-1356986-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356986
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356986
    reference: chr 19
allele count: 1
allele frequency: 8.622622311897494e-6
allele num: 115974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.10T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-22T>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-22T>G
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-1356990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1356990
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1356990
    reference: chr 19
allele count: 2
allele frequency: 1.713766687803123e-5
allele num: 116702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.14C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-18C>A
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff

19-1357003-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357003
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357003
    reference: chr 19
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.27T>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-5T>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.61-5T>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

19-1357005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357005
    reference: chr 19
allele count: 1
allele frequency: 8.360365180751095e-6
allele num: 119612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.226-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.29T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-260-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.43-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.61-3T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.61-3T>C
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

19-1357017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357017
    reference: chr 19
allele count: 2
allele frequency: 1.658209796703479e-5
allele num: 120612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-251C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.70C>T
  hgvsp: ENSP00000345789.3:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.52C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.70C>T
  hgvsp: ENSP00000394925.2:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.70C>T
  hgvsp: ENSP00000468557.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.70C>T
  hgvsp: ENSP00000467083.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.70C>T
  hgvsp: ENSP00000465838.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.70C>T
  hgvsp: ENSP00000467287.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.70C>T
  hgvsp: ENSP00000466891.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.70C>T
  hgvsp: ENSP00000468322.1:p.Arg24Ter
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.235C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.41C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Ter
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

19-1357018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357018
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357018
    reference: chr 19
allele count: 101
allele frequency: 8.368547518435662e-4
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.71G>A
  hgvsp: ENSP00000466891.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.71G>A
  hgvsp: ENSP00000468322.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-250G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.53G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.42G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.71G>A
  hgvsp: ENSP00000467287.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.71G>A
  hgvsp: ENSP00000467083.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.71G>A
  hgvsp: ENSP00000465838.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.71G>A
  hgvsp: ENSP00000345789.3:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.71G>A
  hgvsp: ENSP00000468557.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.71G>A
  hgvsp: ENSP00000394925.2:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.236G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34832
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Gln
num of homozygotes: 2
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

19-1357022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357022
    reference: chr 19
allele count: 2
allele frequency: 1.655382476121108e-5
allele num: 120818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.75C>T
  hgvsp: ENST00000415183.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.75C>T
  hgvsp: ENST00000591337.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-246C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.240C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.75C>T
  hgvsp: ENST00000591806.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.75C>T
  hgvsp: ENST00000587460.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.57C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.75C>T
  hgvsp: ENST00000588810.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.75C>T
  hgvsp: ENST00000344663.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.75C>T
  hgvsp: ENST00000591433.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.75C>T
  hgvsp: ENST00000592374.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.46C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr25Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

19-1357023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357023
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357023
    reference: chr 19
allele count: 2
allele frequency: 1.654998924250699e-5
allele num: 120846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.241G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.76G>A
  hgvsp: ENSP00000468322.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.76G>A
  hgvsp: ENSP00000467287.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.76G>A
  hgvsp: ENSP00000465838.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.76G>A
  hgvsp: ENSP00000468557.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-245G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.76G>A
  hgvsp: ENSP00000467083.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.47G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.58G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.76G>A
  hgvsp: ENSP00000466891.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.76G>A
  hgvsp: ENSP00000345789.3:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.76G>A
  hgvsp: ENSP00000394925.2:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34777
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala26Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-1357025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357025
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357025
    reference: chr 19
allele count: 61
allele frequency: 5.04524175805998e-4
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.78G>A
  hgvsp: ENST00000591337.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.78G>A
  hgvsp: ENST00000591806.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.78G>A
  hgvsp: ENST00000591433.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.60G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.78G>A
  hgvsp: ENST00000592374.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.78G>A
  hgvsp: ENST00000587460.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.243G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.78G>A
  hgvsp: ENST00000415183.3:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.78G>A
  hgvsp: ENST00000588810.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.49G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-243G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.78G>A
  hgvsp: ENST00000344663.3:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34711
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Ala26Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-1357028-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357028
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357028
    reference: chr 19
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.246T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.81T>C
  hgvsp: ENST00000587460.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.81T>C
  hgvsp: ENST00000588810.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.81T>C
  hgvsp: ENST00000344663.3:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.81T>C
  hgvsp: ENST00000591433.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-240T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.81T>C
  hgvsp: ENST00000591806.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.81T>C
  hgvsp: ENST00000592374.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.63T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.81T>C
  hgvsp: ENST00000591337.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.81T>C
  hgvsp: ENST00000415183.3:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.52T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr27Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

19-1357032-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357032
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357032
    reference: chr 19
allele count: 4
allele frequency: 3.304965710980749e-5
allele num: 121030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.85A>G
  hgvsp: ENSP00000465838.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.85A>G
  hgvsp: ENSP00000468322.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.56A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.85A>G
  hgvsp: ENSP00000468557.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.250A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.85A>G
  hgvsp: ENSP00000394925.2:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.85A>G
  hgvsp: ENSP00000467083.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.85A>G
  hgvsp: ENSP00000467287.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.85A>G
  hgvsp: ENSP00000466891.1:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-236A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.67A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.85A>G
  hgvsp: ENSP00000345789.3:p.Thr29Ala
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr29Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-1357033-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357032
    reference: chr 19
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.92delA
  hgvsp: ENSP00000468322.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.257delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.92delA
  hgvsp: ENSP00000465838.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.92delA
  hgvsp: ENSP00000394925.2:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.63delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.92delA
  hgvsp: ENSP00000468557.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.92delA
  hgvsp: ENSP00000467083.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.92delA
  hgvsp: ENSP00000345789.3:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.92delA
  hgvsp: ENSP00000466891.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.74delA
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.92delA
  hgvsp: ENSP00000467287.1:p.Asn31IlefsTer9
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-229delA
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn31IlefsTer9
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: CA
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

19-1357039-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357039
    reference: chr 19
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.257A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.92A>G
  hgvsp: ENSP00000468322.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.92A>G
  hgvsp: ENSP00000394925.2:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.92A>G
  hgvsp: ENSP00000466891.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.74A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.63A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.92A>G
  hgvsp: ENSP00000467083.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.92A>G
  hgvsp: ENSP00000465838.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.92A>G
  hgvsp: ENSP00000468557.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-229A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.92A>G
  hgvsp: ENSP00000345789.3:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.92A>G
  hgvsp: ENSP00000467287.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn31Ser
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

19-1357042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357042
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357042
    reference: chr 19
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.95A>G
  hgvsp: ENSP00000394925.2:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.95A>G
  hgvsp: ENSP00000468322.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.95A>G
  hgvsp: ENSP00000345789.3:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.95A>G
  hgvsp: ENSP00000467083.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.260A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.95A>G
  hgvsp: ENSP00000468557.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.95A>G
  hgvsp: ENSP00000466891.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-226A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.95A>G
  hgvsp: ENSP00000465838.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.95A>G
  hgvsp: ENSP00000467287.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.66A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.77A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys32Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

19-1357044-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357044
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357044
    reference: chr 19
allele count: 3
allele frequency: 2.476718842876956e-5
allele num: 121128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.97A>G
  hgvsp: ENSP00000467287.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.97A>G
  hgvsp: ENSP00000345789.3:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.68A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.79A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.97A>G
  hgvsp: ENSP00000465838.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.97A>G
  hgvsp: ENSP00000468322.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.97A>G
  hgvsp: ENSP00000468557.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.97A>G
  hgvsp: ENSP00000394925.2:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.262A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.97A>G
  hgvsp: ENSP00000466891.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-224A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.97A>G
  hgvsp: ENSP00000467083.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg33Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-1357048-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357048
    reference: chr 19
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.101G>C
  hgvsp: ENSP00000468557.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.83G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.72G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.101G>C
  hgvsp: ENSP00000465838.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.101G>C
  hgvsp: ENSP00000466891.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-220G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.266G>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.101G>C
  hgvsp: ENSP00000345789.3:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.101G>C
  hgvsp: ENSP00000394925.2:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.101G>C
  hgvsp: ENSP00000468322.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.101G>C
  hgvsp: ENSP00000467083.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.101G>C
  hgvsp: ENSP00000467287.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg34Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-1357048-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357048
    reference: chr 19
allele count: 8
allele frequency: 6.603820310049364e-5
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.101G>T
  hgvsp: ENSP00000468557.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.83G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.101G>T
  hgvsp: ENSP00000394925.2:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.101G>T
  hgvsp: ENSP00000465838.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.266G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.101G>T
  hgvsp: ENSP00000466891.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.101G>T
  hgvsp: ENSP00000345789.3:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.101G>T
  hgvsp: ENSP00000467083.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.101G>T
  hgvsp: ENSP00000467287.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.72G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-220G>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.101G>T
  hgvsp: ENSP00000468322.1:p.Arg34Ile
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg34Ile
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

19-1357052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357052
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357052
    reference: chr 19
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.87G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.105G>A
  hgvsp: ENST00000344663.3:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.105G>A
  hgvsp: ENST00000588810.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-216G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.105G>A
  hgvsp: ENST00000592374.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.105G>A
  hgvsp: ENST00000415183.3:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.105G>A
  hgvsp: ENST00000587460.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.105G>A
  hgvsp: ENST00000591337.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.270G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.105G>A
  hgvsp: ENST00000591433.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.76G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.105G>A
  hgvsp: ENST00000591806.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys35Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/19-1357055-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357055
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357055
    reference: chr 19
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.79A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.108A>C
  hgvsp: ENSP00000467287.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-213A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.90A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.108A>C
  hgvsp: ENSP00000468557.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.108A>C
  hgvsp: ENSP00000466891.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.108A>C
  hgvsp: ENSP00000467083.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.108A>C
  hgvsp: ENSP00000394925.2:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.108A>C
  hgvsp: ENSP00000468322.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.108A>C
  hgvsp: ENSP00000465838.1:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.273A>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.108A>C
  hgvsp: ENSP00000345789.3:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu36Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-1357066-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357066
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357066
    reference: chr 19
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.119C>A
  hgvsp: ENSP00000394925.2:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.119C>A
  hgvsp: ENSP00000468322.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.101C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.119C>A
  hgvsp: ENSP00000466891.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.119C>A
  hgvsp: ENSP00000345789.3:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.119C>A
  hgvsp: ENSP00000467083.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.119C>A
  hgvsp: ENSP00000468557.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.119C>A
  hgvsp: ENSP00000465838.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-202C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.90C>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.119C>A
  hgvsp: ENSP00000467287.1:p.Ala40Asp
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.284C>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala40Asp
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-1357082-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357082
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357082
    reference: chr 19
allele count: 90821
allele frequency: 7.491998284168152e-1
allele num: 121224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.135T>C
  hgvsp: ENST00000591337.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.135T>C
  hgvsp: ENST00000588810.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.135T>C
  hgvsp: ENST00000591433.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.135T>C
  hgvsp: ENST00000591806.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.135T>C
  hgvsp: ENST00000415183.3:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.135T>C
  hgvsp: ENST00000344663.3:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.300T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-186T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000466891
  ensembl transcript: ENST00000592374
  gene symbol: MUM1
  hgvsc: ENST00000592374.1:c.135T>C
  hgvsp: ENST00000592374.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.117T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.135T>C
  hgvsp: ENST00000587460.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.106T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.25e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 5174
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 9.75e1
  variant carriers: 8886
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 9.25e1
  variant carriers: 1664
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 3220
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 6.75e1
  variant carriers: 4751
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 3.75e1
  variant carriers: 2309
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 8.25e1
  variant carriers: 2879
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 6.25e1
  variant carriers: 5233
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 4.75e1
  variant carriers: 4176
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.25e1
  variant carriers: 1475
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 7.75e1
  variant carriers: 3667
genotype quality: GenotypeQuality
hgvs: p.Ser45Ser
num of homozygotes: 34416
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP

19-1357101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357101
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357101
    reference: chr 19
allele count: 8
allele frequency: 6.697026520225021e-5
allele num: 119456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.319G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.125G>A
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+8G>A
  variant of: http://identifiers.org/hgnc/29641
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14652
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.146+8G>A
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: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

19-1357102-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357102
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357102
    reference: chr 19
allele count: 1
allele frequency: 8.382932349735938e-6
allele num: 119290
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.126T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.320T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+9T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

19-1357117-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357117
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357117
    reference: chr 19
allele count: 1
allele frequency: 8.460523198754612e-6
allele num: 118196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.335A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.141A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+24A>G
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+24A>G
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

19-1357120-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357120
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357121
    reference: chr 19
allele count: 1
allele frequency: 8.504269143109841e-6
allele num: 117588
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.150dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.344dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+33dupT
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18120
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

19-1357121-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357121
    reference: chr 19
allele count: 19
allele frequency: 1.615426472588763e-4
allele num: 117616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.145T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.339T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+28T>C
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+28T>C
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12492
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18170
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

19-1357128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1357128
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1357128
    reference: chr 19
allele count: 3
allele frequency: 2.566252074387094e-5
allele num: 116902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000588351
  gene symbol: MUM1
  hgvsc: ENST00000588351.1:n.346C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590866
  gene symbol: MUM1
  hgvsc: ENST00000590866.1:n.128+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000309135
  ensembl transcript: ENST00000311401
  gene symbol: MUM1
  hgvsc: ENST00000311401.5:c.-175+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467287
  ensembl transcript: ENST00000591337
  gene symbol: MUM1
  hgvsc: ENST00000591337.1:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000160953
  ensembl transcript: ENST00000590695
  gene symbol: MUM1
  hgvsc: ENST00000590695.1:n.152C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468322
  ensembl transcript: ENST00000591433
  gene symbol: MUM1
  hgvsc: ENST00000591433.1:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000394925
  ensembl transcript: ENST00000415183
  gene symbol: MUM1
  hgvsc: ENST00000415183.3:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000468557
  ensembl transcript: ENST00000588810
  gene symbol: MUM1
  hgvsc: ENST00000588810.1:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000467083
  ensembl transcript: ENST00000591806
  gene symbol: MUM1
  hgvsc: ENST00000591806.1:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000465838
  ensembl transcript: ENST00000587460
  gene symbol: MUM1
  hgvsc: ENST00000587460.1:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160953
  ensembl protein: ENSP00000345789
  ensembl transcript: ENST00000344663
  gene symbol: MUM1
  hgvsc: ENST00000344663.3:c.146+35C>T
  variant of: http://identifiers.org/hgnc/29641
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
reference allele: C

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

GenotypeQuality
all individuals: 652
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24109
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15902
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.053641105680371e-5
allele num: 48694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.269146e6

VQSLOD
type: SiteQuality
SIO_000300: -2.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.348e1

GenotypeQuality
all individuals: 178
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 5
allele frequency: 7.621951219512195e-4
allele num: 6560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.548946716232962e-4
allele num: 12912
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50090
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.549e1

DP
type: SiteQuality
SIO_000300: 1.296852e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.063e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

GenotypeQuality
all individuals: 3416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3839
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.527853056308341e-5
allele num: 13284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52534
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

DP
type: SiteQuality
SIO_000300: 1.339555e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.064e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

FS
type: SiteQuality
SIO_000300: 4.201e0

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

GenotypeQuality
all individuals: 1323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9544
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3853
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 7.211885186787827e-5
allele num: 13866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

DP
type: SiteQuality
SIO_000300: 1.412474e6

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

FS
type: SiteQuality
SIO_000300: 1.522e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

GenotypeQuality
all individuals: 466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34137
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3853
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084128360797918e-4
allele num: 9224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14010
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.442e0

DP
type: SiteQuality
SIO_000300: 1.424777e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.399e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.096e0

QD
type: SiteQuality
SIO_000300: 3.104e1

GenotypeQuality
all individuals: 7782
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35270
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 462
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 659
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 7.75e1
variant carriers: 1

South Asian
type: Population
allele count: 2
allele frequency: 1.410437235543018e-4
allele num: 14180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.404718940451466e-5
allele num: 58742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

Latino
type: Population
allele count: 26
allele frequency: 2.73972602739726e-3
allele num: 9490
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.740648379052369e-3
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 522
allele frequency: 5.750165234633179e-2
allele num: 9078
num of homozygotes: 14

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

FS
type: SiteQuality
SIO_000300: 8.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.808e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.458545e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

GenotypeQuality
all individuals: 523
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3906
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1473
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.023458350891979e-5
allele num: 14238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

FS
type: SiteQuality
SIO_000300: 1.327e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

QD
type: SiteQuality
SIO_000300: 8.609999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

DP
type: SiteQuality
SIO_000300: 1.458033e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4229
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.680502806439687e-5
allele num: 59506
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.067397146991937e-4
allele num: 9674
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.465687e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.94637399277577e-5
allele num: 14396
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.492e0

DP
type: SiteQuality
SIO_000300: 1.474098e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.073e0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579479403588577e-5
allele num: 63312
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.343e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.73e-1

DP
type: SiteQuality
SIO_000300: 1.546942e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.928385107896609e-4
allele num: 8434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10834
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

QD
type: SiteQuality
SIO_000300: 1.033e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.214e0

MQ
type: SiteQuality
SIO_000300: 6.007e1

DP
type: SiteQuality
SIO_000300: 1.561748e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.547987616099071e-4
allele num: 6460
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.574818e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 1
allele frequency: 1.531393568147014e-4
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65202
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.196e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

DP
type: SiteQuality
SIO_000300: 1.591836e6

MQ
type: SiteQuality
SIO_000300: 5.829e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.299e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8636
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.940993788819876e-4
allele num: 10304
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.619809e6

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.61e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 487
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66370
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.413e0

ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

DP
type: SiteQuality
SIO_000300: 1.624345e6

FS
type: SiteQuality
SIO_000300: 7.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.025e0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 5224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.046e0

FS
type: SiteQuality
SIO_000300: 2.494e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.891e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.023e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.625913e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1096
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.823264859608606e-4
allele num: 16454
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: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.628991e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.232e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 488
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GenotypeQuality
all individuals: 45595
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66482
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.19e-2

MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

DP
type: SiteQuality
SIO_000300: 1.629079e6

QD
type: SiteQuality
SIO_000300: 1.081e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.992e0

VQSLOD
type: SiteQuality
SIO_000300: -4.314e-1

FS
type: SiteQuality
SIO_000300: 2.027e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.629363e6

QD
type: SiteQuality
SIO_000300: 9.23e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 36
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

FS
type: SiteQuality
SIO_000300: 2.787e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.629455e6

QD
type: SiteQuality
SIO_000300: 9.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.185e0

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.012686769082765e-5
allele num: 66526
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
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BaseQRankSum
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SIO_000300: -3.372e0

MQ
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ClippingRankSum
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FS
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

South Asian
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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: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Other
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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 count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

African
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num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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SIO_000300: 7.63e0

MQ
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

African
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allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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MQ
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DP
type: SiteQuality
SIO_000300: 1.632149e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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 frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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DP
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SIO_000300: 1.632146e6

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

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

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: 8646
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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allele num: 10386
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DP
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SIO_000300: 1.63279e6

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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FS
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VQSLOD
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SIO_000300: -2.111e0

InbreedingCoeff
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SIO_000300: 1.0e-4

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

European (Finnish)
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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 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

East Asian
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allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
num of homozygotes: 0

African
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BaseQRankSum
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SIO_000300: 3.35e0

DP
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VQSLOD
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

East Asian
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Other
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Latino
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 2

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: 3

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.775338928340865e-3
allele num: 6196
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.477656059815684e-4
allele num: 11502
num of homozygotes: 0

East Asian
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allele frequency: 1.16795141322121e-4
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European (Non-Finnish)
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allele count: 35
allele frequency: 5.370239666124528e-4
allele num: 65174
num of homozygotes: 0

African
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Other
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South Asian
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FS
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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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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variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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African
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East Asian
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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SIO_000300: -2.2e-1

DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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QD
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SIO_000300: 8.029999999999999e0

MQ
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SIO_000300: 5.858e1

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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Other
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East Asian
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66516
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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ReadPosRankSum
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DP
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VQSLOD
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QD
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FS
type: SiteQuality
SIO_000300: 2.234e0

MQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.982e1

ClippingRankSum
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BaseQRankSum
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SIO_000300: -3.818e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8642
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
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Other
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African
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South Asian
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

BaseQRankSum
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SIO_000300: 3.16e0

DP
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SIO_000300: 1.667062e6

VQSLOD
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SIO_000300: -2.195e0

ClippingRankSum
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SIO_000300: -8.76e-1

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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 4.630701551285019e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11522
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Other
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South Asian
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ClippingRankSum
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SIO_000300: 1.08e-1

MQRankSum
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 66416
num of homozygotes: 0

African
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South Asian
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Other
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European (Finnish)
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East Asian
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Latino
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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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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European (Non-Finnish)
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allele num: 66370
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East Asian
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European (Finnish)
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South Asian
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Latino
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Other
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African
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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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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num of homozygotes: 0

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

South Asian
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allele count: 14
allele frequency: 8.536585365853659e-4
allele num: 16400
num of homozygotes: 0

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

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

BaseQRankSum
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SIO_000300: 2.76e0

MQRankSum
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DP
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ClippingRankSum
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SIO_000300: 4.0e-1

ReadPosRankSum
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MQ
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FS
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QD
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SIO_000300: 1.446e1

InbreedingCoeff
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SIO_000300: 1.5e-3

VQSLOD
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SIO_000300: 5.16e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 57

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
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allele count: 56
allele frequency: 5.446411204045905e-3
allele num: 10282
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Other
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allele count: 0
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ReadPosRankSum
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SIO_000300: 3.94e-1

MQ
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QD
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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SIO_000300: 1.9e-3

FS
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BaseQRankSum
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VQSLOD
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SIO_000300: 6.54e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 9.305788200260562e-5
allele num: 10746
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61716
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 2

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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variant carriers: 59

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 62852
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8082
num of homozygotes: 0

Latino
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allele frequency: 3.650301149844862e-4
allele num: 10958
num of homozygotes: 0

South Asian
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Other
type: Population
allele count: 0
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African
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allele frequency: 5.489021956087825e-3
allele num: 10020
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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DP
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.97e-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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.576193178235924e-5
allele num: 63444
num of homozygotes: 0

Other
type: Population
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African
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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

European (Finnish)
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East Asian
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South Asian
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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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BaseQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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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
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

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

Latino
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allele num: 11522
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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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South Asian
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VQSLOD
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DP
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FS
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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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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.471418653089562e-4
allele num: 8642
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.254e0

ClippingRankSum
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SIO_000300: 6.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.62e-1

DP
type: SiteQuality
SIO_000300: 1.972596e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

FS
type: SiteQuality
SIO_000300: 3.1801e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 1.717e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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: 16492
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
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
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.973208e6

VQSLOD
type: SiteQuality
SIO_000300: -7.862e-1

InbreedingCoeff
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SIO_000300: 2.0e-4

FS
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SIO_000300: 1.8832e1

BaseQRankSum
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SIO_000300: -6.820000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-2

QD
type: SiteQuality
SIO_000300: 9.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

MQ
type: SiteQuality
SIO_000300: 6.008e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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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: 10328
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.37e-1

FS
type: SiteQuality
SIO_000300: 7.627e0

DP
type: SiteQuality
SIO_000300: 1.974084e6

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeDepth
all individuals: 302
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

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

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

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
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
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

InbreedingCoeff
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DP
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QD
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MQ
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BaseQRankSum
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MQRankSum
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SIO_000300: 2.95e-1

ClippingRankSum
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SIO_000300: 1.29e0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.6e0

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

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

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

South Asian
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allele count: 3
allele frequency: 1.818402230573403e-4
allele num: 16498
num of homozygotes: 0

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

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

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

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

BaseQRankSum
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SIO_000300: 4.46e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

South Asian
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allele count: 1
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allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

Other
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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VQSLOD
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MQ
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QD
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InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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GenotypeDepth
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variant carriers: 3

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

African
type: Population
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.505451596431682e-5
allele num: 66586
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 5
allele frequency: 7.562008469449486e-4
allele num: 6612
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.211e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 1.975596e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 2.593e0

QD
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SIO_000300: 1.15e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.864e0

MQ
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SIO_000300: 5.924e1

DP
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SIO_000300: 1.976001e6

MQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

ReadPosRankSum
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SIO_000300: 7.099999999999999e-2

FS
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SIO_000300: 2.952e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.893e1

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.252e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-1

ClippingRankSum
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SIO_000300: 1.06e0

DP
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SIO_000300: 1.976168e6

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.704e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 2866
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.659e0

FS
type: SiteQuality
SIO_000300: 8.116e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.623e0

MQRankSum
type: SiteQuality
SIO_000300: -1.082e0

QD
type: SiteQuality
SIO_000300: 3.163e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.073e0

DP
type: SiteQuality
SIO_000300: 1.976611e6

GenotypeDepth
all individuals: 4265
bin: 7.25e1
variant carriers: 4256

GenotypeDepth
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bin: 2.75e1
variant carriers: 907

GenotypeDepth
all individuals: 2186
bin: 8.75e1
variant carriers: 2173

GenotypeDepth
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variant carriers: 4909

GenotypeQuality
all individuals: 2984
bin: 6.25e1
variant carriers: 128

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 422
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variant carriers: 381

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 26

GenotypeQuality
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bin: 2.25e1
variant carriers: 19

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 571
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variant carriers: 148

GenotypeQuality
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bin: 2.75e1
variant carriers: 16

GenotypeQuality
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variant carriers: 111

GenotypeQuality
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GenotypeQuality
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variant carriers: 45

GenotypeQuality
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GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 68

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 9

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 19

GenotypeQuality
all individuals: 217
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variant carriers: 179

GenotypeQuality
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variant carriers: 54746

GenotypeQuality
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variant carriers: 207

GenotypeQuality
all individuals: 377
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variant carriers: 278

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 23

East Asian
type: Population
allele count: 4638
allele frequency: 5.371785962473941e-1
allele num: 8634
num of homozygotes: 1259

European (Non-Finnish)
type: Population
allele count: 52457
allele frequency: 7.868392632147357e-1
allele num: 66668
num of homozygotes: 20688

South Asian
type: Population
allele count: 12364
allele frequency: 7.495150339476236e-1
allele num: 16496
num of homozygotes: 4653

Latino
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allele count: 8702
allele frequency: 7.519875561700656e-1
allele num: 11572
num of homozygotes: 3291

European (Finnish)
type: Population
allele count: 4333
allele frequency: 6.557203389830508e-1
allele num: 6608
num of homozygotes: 1424

Other
type: Population
allele count: 647
allele frequency: 7.141280353200883e-1
allele num: 906
num of homozygotes: 230

African
type: Population
allele count: 7680
allele frequency: 7.427466150870407e-1
allele num: 10340
num of homozygotes: 2871

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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QD
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SIO_000300: 2.659e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.549171e6

GenotypeDepth
all individuals: 139
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variant carriers: 0

GenotypeDepth
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 1031
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.210250824483374e-4
allele num: 66102
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.975e1

MQRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -5.0e-4

QD
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FS
type: SiteQuality
SIO_000300: 5.3e-1

ReadPosRankSum
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SIO_000300: 9.9e-2

BaseQRankSum
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DP
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SIO_000300: 2.433901e6

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66062
num of homozygotes: 0

East Asian
type: Population
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allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.869e1

MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 4.4e-3

ClippingRankSum
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FS
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BaseQRankSum
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SIO_000300: 3.76e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7457
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GenotypeQuality
all individuals: 1488
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523090045083465e-5
allele num: 65656
num of homozygotes: 0

Latino
type: Population
allele count: 0
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num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.368473e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.846e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

VQSLOD
type: SiteQuality
SIO_000300: -6.839e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

GenotypeQuality
all individuals: 1017
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1488
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1436
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527463799107961e-5
allele num: 65468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14668
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.816e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.75e-1

DP
type: SiteQuality
SIO_000300: 2.330189e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
type: SiteQuality
SIO_000300: 8.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

GenotypeQuality
all individuals: 2087
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3943
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9386
bin: 9.75e1
variant carriers: 19

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

GenotypeQuality
all individuals: 457
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6697
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.985945615643141e-4
allele num: 65460
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.575757575757576e-4
allele num: 6600
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: 14690
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.472e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

DP
type: SiteQuality
SIO_000300: 2.329012e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

GenotypeQuality
all individuals: 347
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9368
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 9.25e1
variant carriers: 0

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