5-66300946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66300946
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66300946
    reference: chr 5
allele count: 3
allele frequency: 1.075191742527417e-4
allele num: 27902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.92+33A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-49286A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-49286A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-49286A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.92+33A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.128+41331A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-49286A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.92+33A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.47+45824A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22487
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20167
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15659
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3515
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

5-66350184-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350184
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350184
    reference: chr 5
allele count: 1
allele frequency: 3.261365860022177e-5
allele num: 30662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-48T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9281
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

5-66350196-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350196
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350196
    reference: chr 5
allele count: 1
allele frequency: 3.156167150612296e-5
allele num: 31684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-36T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-36T>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3506
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

5-66350198-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350198
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350198
    reference: chr 5
allele count: 17
allele frequency: 5.324813631522897e-4
allele num: 31926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-34T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-34T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27645
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16124
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3695
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13510
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

5-66350207-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350207
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350207
    reference: chr 5
allele count: 11
allele frequency: 3.219575016097875e-4
allele num: 34166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-25T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-25T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32184
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9752
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 29506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

5-66350209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350209
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350209
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 34654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-23T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-23T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32877
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

5-66350209-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350209
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350209
    reference: chr 5
allele count: 6
allele frequency: 1.731401858371328e-4
allele num: 34654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-23T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-23T>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32877
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5828
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

5-66350210-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350210
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350211
    reference: chr 5
allele count: 2
allele frequency: 5.757715338553662e-5
allele num: 34736
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-16dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-16dupT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30918
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8590
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

5-66350210-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350210
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350212
    reference: chr 5
allele count: 1
allele frequency: 2.878857669276831e-5
allele num: 34736
alternate allele: GTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-17_675-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-17_93-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-17_675-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-17_48-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-17_129-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-17_93-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-17_108-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-17_108-16dupTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-17_93-16dupTT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30918
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

5-66350217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350217
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350217
    reference: chr 5
allele count: 1
allele frequency: 2.634907251264755e-5
allele num: 37952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-15C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-15C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

5-66350220-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350220
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350220
    reference: chr 5
allele count: 1
allele frequency: 2.455916302372415e-5
allele num: 40718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-12T>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-12T>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

5-66350223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350223
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350223
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 43836
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-9T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-9T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34796
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

5-66350228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350228
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350228
    reference: chr 5
allele count: 1
allele frequency: 1.988071570576541e-5
allele num: 50300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.108-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.129-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.48-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.108-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.93-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.675-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.93-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.93-4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.675-4A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
hgvs: c.675-4A>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

5-66350239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350239
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350239
    reference: chr 5
allele count: 1
allele frequency: 1.4972301242701e-5
allele num: 66790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.55A>G
  hgvsp: ENSP00000413854.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.682A>G
  hgvsp: ENSP00000385727.1:p.Thr228Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.100A>G
  hgvsp: ENSP00000398694.1:p.Thr34Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.136A>G
  hgvsp: ENSP00000384099.1:p.Thr46Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.115A>G
  hgvsp: ENSP00000384313.1:p.Thr39Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.100A>G
  hgvsp: ENSP00000392478.1:p.Thr34Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.115A>G
  hgvsp: ENSP00000421739.1:p.Thr39Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.682A>G
  hgvsp: ENSP00000385048.3:p.Thr228Ala
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.100A>G
  hgvsp: ENSP00000261569.7:p.Thr34Ala
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr228Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

5-66350242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350242
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350242
    reference: chr 5
allele count: 1
allele frequency: 1.427551748750892e-5
allele num: 70050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.103A>G
  hgvsp: ENSP00000398694.1:p.Ser35Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.118A>G
  hgvsp: ENSP00000421739.1:p.Ser40Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.103A>G
  hgvsp: ENSP00000261569.7:p.Ser35Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.118A>G
  hgvsp: ENSP00000384313.1:p.Ser40Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.103A>G
  hgvsp: ENSP00000392478.1:p.Ser35Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.685A>G
  hgvsp: ENSP00000385727.1:p.Ser229Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.58A>G
  hgvsp: ENSP00000413854.1:p.Ser20Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.685A>G
  hgvsp: ENSP00000385048.3:p.Ser229Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.139A>G
  hgvsp: ENSP00000384099.1:p.Ser47Gly
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24805
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser229Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

5-66350249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350249
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350249
    reference: chr 5
allele count: 15
allele frequency: 1.936383352266859e-4
allele num: 77464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.110G>A
  hgvsp: ENSP00000392478.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.692G>A
  hgvsp: ENSP00000385048.3:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.110G>A
  hgvsp: ENSP00000398694.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.125G>A
  hgvsp: ENSP00000384313.1:p.Arg42Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.110G>A
  hgvsp: ENSP00000261569.7:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.692G>A
  hgvsp: ENSP00000385727.1:p.Arg231Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.125G>A
  hgvsp: ENSP00000421739.1:p.Arg42Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.65G>A
  hgvsp: ENSP00000413854.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.146G>A
  hgvsp: ENSP00000384099.1:p.Arg49Gln
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25725
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg231Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

5-66350256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350256
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350256
    reference: chr 5
allele count: 1
allele frequency: 1.198121345729895e-5
allele num: 83464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.699C>T
  hgvsp: ENST00000404260.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.117C>T
  hgvsp: ENST00000447738.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.72C>T
  hgvsp: ENST00000432426.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.117C>T
  hgvsp: ENST00000436277.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.153C>T
  hgvsp: ENST00000405643.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.132C>T
  hgvsp: ENST00000403666.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.117C>T
  hgvsp: ENST00000261569.7:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.699C>T
  hgvsp: ENST00000403625.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.132C>T
  hgvsp: ENST00000490016.2:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser233Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

5-66350270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350270
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350270
    reference: chr 5
allele count: 1
allele frequency: 1.092227707632487e-5
allele num: 91556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.131G>A
  hgvsp: ENSP00000398694.1:p.Gly44Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.131G>A
  hgvsp: ENSP00000392478.1:p.Gly44Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.86G>A
  hgvsp: ENSP00000413854.1:p.Gly29Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.167G>A
  hgvsp: ENSP00000384099.1:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.713G>A
  hgvsp: ENSP00000385048.3:p.Gly238Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.146G>A
  hgvsp: ENSP00000421739.1:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.713G>A
  hgvsp: ENSP00000385727.1:p.Gly238Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.131G>A
  hgvsp: ENSP00000261569.7:p.Gly44Glu
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.146G>A
  hgvsp: ENSP00000384313.1:p.Gly49Glu
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31918
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly238Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS

5-66350283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350283
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350283
    reference: chr 5
allele count: 1
allele frequency: 1.062044648357017e-5
allele num: 94158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.726A>G
  hgvsp: ENST00000404260.3:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.99A>G
  hgvsp: ENST00000432426.1:c.99A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.144A>G
  hgvsp: ENST00000447738.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.159A>G
  hgvsp: ENST00000490016.2:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.159A>G
  hgvsp: ENST00000403666.1:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.726A>G
  hgvsp: ENST00000403625.2:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.144A>G
  hgvsp: ENST00000436277.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.144A>G
  hgvsp: ENST00000261569.7:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.180A>G
  hgvsp: ENST00000405643.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33271
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala242Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

5-66350290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350290
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350290
    reference: chr 5
allele count: 2
allele frequency: 2.143668674569658e-5
allele num: 93298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.151C>T
  hgvsp: ENSP00000261569.7:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.106C>T
  hgvsp: ENSP00000413854.1:p.Arg36Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.733C>T
  hgvsp: ENSP00000385727.1:p.Arg245Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.151C>T
  hgvsp: ENSP00000392478.1:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.733C>T
  hgvsp: ENSP00000385048.3:p.Arg245Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.166C>T
  hgvsp: ENSP00000384313.1:p.Arg56Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.166C>T
  hgvsp: ENSP00000421739.1:p.Arg56Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.187C>T
  hgvsp: ENSP00000384099.1:p.Arg63Ter
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.151C>T
  hgvsp: ENSP00000398694.1:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29266
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg245Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

5-66350291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350291
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350291
    reference: chr 5
allele count: 2
allele frequency: 2.141144227475163e-5
allele num: 93408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.734G>A
  hgvsp: ENSP00000385048.3:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.152G>A
  hgvsp: ENSP00000398694.1:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.152G>A
  hgvsp: ENSP00000392478.1:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.152G>A
  hgvsp: ENSP00000261569.7:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.188G>A
  hgvsp: ENSP00000384099.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.167G>A
  hgvsp: ENSP00000384313.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.167G>A
  hgvsp: ENSP00000421739.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.734G>A
  hgvsp: ENSP00000385727.1:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.107G>A
  hgvsp: ENSP00000413854.1:p.Arg36Gln
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16514
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg245Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/5-66350297-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350297
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350297
    reference: chr 5
allele count: 1
allele frequency: 1.08201687946332e-5
allele num: 92420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.173A>C
  hgvsp: ENSP00000421739.1:p.His58Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.158A>C
  hgvsp: ENSP00000392478.1:p.His53Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.194A>C
  hgvsp: ENSP00000384099.1:p.His65Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.113A>C
  hgvsp: ENSP00000413854.1:p.His38Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.173A>C
  hgvsp: ENSP00000384313.1:p.His58Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.740A>C
  hgvsp: ENSP00000385048.3:p.His247Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.158A>C
  hgvsp: ENSP00000261569.7:p.His53Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.740A>C
  hgvsp: ENSP00000385727.1:p.His247Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.158A>C
  hgvsp: ENSP00000398694.1:p.His53Pro
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His247Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

5-66350302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350302
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350302
    reference: chr 5
allele count: 1
allele frequency: 1.102779003087781e-5
allele num: 90680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.163C>T
  hgvsp: ENSP00000392478.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.178C>T
  hgvsp: ENSP00000421739.1:p.Pro60Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.745C>T
  hgvsp: ENSP00000385727.1:p.Pro249Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.199C>T
  hgvsp: ENSP00000384099.1:p.Pro67Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.163C>T
  hgvsp: ENSP00000261569.7:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.745C>T
  hgvsp: ENSP00000385048.3:p.Pro249Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.118C>T
  hgvsp: ENSP00000413854.1:p.Pro40Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.178C>T
  hgvsp: ENSP00000384313.1:p.Pro60Ser
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.163C>T
  hgvsp: ENSP00000398694.1:p.Pro55Ser
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro249Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

5-66350306-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350306
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350306
    reference: chr 5
allele count: 1
allele frequency: 1.114156472134947e-5
allele num: 89754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.182T>A
  hgvsp: ENSP00000384313.1:p.Leu61His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.167T>A
  hgvsp: ENSP00000392478.1:p.Leu56His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.182T>A
  hgvsp: ENSP00000421739.1:p.Leu61His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.749T>A
  hgvsp: ENSP00000385727.1:p.Leu250His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.749T>A
  hgvsp: ENSP00000385048.3:p.Leu250His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.203T>A
  hgvsp: ENSP00000384099.1:p.Leu68His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.122T>A
  hgvsp: ENSP00000413854.1:p.Leu41His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.167T>A
  hgvsp: ENSP00000261569.7:p.Leu56His
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.167T>A
  hgvsp: ENSP00000398694.1:p.Leu56His
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu250His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

5-66350314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350314
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350314
    reference: chr 5
allele count: 1
allele frequency: 1.143040029261825e-5
allele num: 87486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.757C>T
  hgvsp: ENSP00000385048.3:p.His253Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.175C>T
  hgvsp: ENSP00000392478.1:p.His59Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.130C>T
  hgvsp: ENSP00000413854.1:p.His44Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.757C>T
  hgvsp: ENSP00000385727.1:p.His253Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.175C>T
  hgvsp: ENSP00000398694.1:p.His59Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.211C>T
  hgvsp: ENSP00000384099.1:p.His71Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.190C>T
  hgvsp: ENSP00000384313.1:p.His64Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.175C>T
  hgvsp: ENSP00000261569.7:p.His59Tyr
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.190C>T
  hgvsp: ENSP00000421739.1:p.His64Tyr
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His253Tyr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

5-66350315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350315
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350315
    reference: chr 5
allele count: 11
allele frequency: 1.265677137268439e-4
allele num: 86910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.191A>G
  hgvsp: ENSP00000384313.1:p.His64Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.176A>G
  hgvsp: ENSP00000392478.1:p.His59Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.758A>G
  hgvsp: ENSP00000385048.3:p.His253Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.758A>G
  hgvsp: ENSP00000385727.1:p.His253Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.191A>G
  hgvsp: ENSP00000421739.1:p.His64Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.176A>G
  hgvsp: ENSP00000398694.1:p.His59Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.212A>G
  hgvsp: ENSP00000384099.1:p.His71Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.176A>G
  hgvsp: ENSP00000261569.7:p.His59Arg
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.131A>G
  hgvsp: ENSP00000413854.1:p.His44Arg
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 19391
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His253Arg
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

5-66350316-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350316
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350316
    reference: chr 5
allele count: 12
allele frequency: 1.393728222996516e-4
allele num: 86100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.132T>G
  hgvsp: ENSP00000413854.1:p.His44Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.177T>G
  hgvsp: ENSP00000398694.1:p.His59Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.177T>G
  hgvsp: ENSP00000261569.7:p.His59Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.192T>G
  hgvsp: ENSP00000384313.1:p.His64Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.192T>G
  hgvsp: ENSP00000421739.1:p.His64Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.177T>G
  hgvsp: ENSP00000392478.1:p.His59Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.759T>G
  hgvsp: ENSP00000385048.3:p.His253Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.213T>G
  hgvsp: ENSP00000384099.1:p.His71Gln
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.759T>G
  hgvsp: ENSP00000385727.1:p.His253Gln
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12965
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16261
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26130
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His253Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

5-66350324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350324
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350324
    reference: chr 5
allele count: 1
allele frequency: 1.212238762546671e-5
allele num: 82492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+4A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+4A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 3.25e1
  variant carriers: 0
hgvs: c.763+4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-66350338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350338
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350338
    reference: chr 5
allele count: 16
allele frequency: 2.114779666393508e-4
allele num: 75658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+18C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+18C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18263
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20656
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

5-66350341-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350341
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350341
    reference: chr 5
allele count: 1
allele frequency: 1.36302919608538e-5
allele num: 73366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+21G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+21G>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20780
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3444
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2372
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

5-66350342-AGTTTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350342
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350337
    reference: chr 5
allele count: 105
allele frequency: 1.440171174631042e-3
allele num: 72908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+28_196+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+28_763+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+28_181+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+28_136+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+28_217+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+28_763+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+28_196+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+28_181+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+28_181+32delGTTTT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18554
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6534
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20781
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31906
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: AGTTTT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

5-66350343-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350343
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350342
    reference: chr 5
allele count: 1
allele frequency: 1.392912859371518e-5
allele num: 71792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+27delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+27delT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5954
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: GT
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

5-66350353-ATTTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66350353
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66350349
    reference: chr 5
allele count: 1
allele frequency: 1.670508836991748e-5
allele num: 59862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.196+37_196+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.181+37_181+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.181+37_181+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.136+37_136+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.196+37_196+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.181+37_181+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.763+37_763+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.217+37_217+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.763+37_763+40delCTTT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10503
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: ATTTC
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

5-66385942-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385942
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385942
    reference: chr 5
allele count: 1
allele frequency: 1.229226079260498e-5
allele num: 81352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-48T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-48T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

5-66385943-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385943
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385943
    reference: chr 5
allele count: 1
allele frequency: 1.234933807547915e-5
allele num: 80976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-47G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-47G>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18765
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4484
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3542
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

5-66385957-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385957
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385957
    reference: chr 5
allele count: 1
allele frequency: 1.207350348924251e-5
allele num: 82826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-33T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-33T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-66385959-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385959
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385959
    reference: chr 5
allele count: 1
allele frequency: 1.201951969999279e-5
allele num: 83198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-31T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-31T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16701
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11344
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16371
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

5-66385967-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385967
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385965
    reference: chr 5
allele count: 2
allele frequency: 2.33639400948576e-5
allele num: 85602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-17_197-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-17_764-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-17_197-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-17_182-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-17_764-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-17_137-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-17_218-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-17_182-16delCT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-17_182-16delCT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14986
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: TTC
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/5-66385969-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385969
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385969
    reference: chr 5
allele count: 1
allele frequency: 1.158453233242974e-5
allele num: 86322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-21C>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-21C>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4099
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

5-66385980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385980
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385980
    reference: chr 5
allele count: 1
allele frequency: 1.058514692183928e-5
allele num: 94472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-10C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-10C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

5-66385986-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66385986
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66385986
    reference: chr 5
allele count: 2
allele frequency: 2.010656479340505e-5
allele num: 99470
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.764-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.764-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.197-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.137-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.182-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.182-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.218-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.197-4C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.182-4C>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30306
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10823
  bin: 2.25e1
  variant carriers: 0
hgvs: c.764-4C>G
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

5-66386019-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386019
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386019
    reference: chr 5
allele count: 1
allele frequency: 8.970540744196061e-6
allele num: 111476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.226T>G
  hgvsp: ENSP00000384313.1:p.Phe76Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.226T>G
  hgvsp: ENSP00000421739.1:p.Phe76Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.211T>G
  hgvsp: ENSP00000398694.1:p.Phe71Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.211T>G
  hgvsp: ENSP00000392478.1:p.Phe71Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.211T>G
  hgvsp: ENSP00000261569.7:p.Phe71Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.166T>G
  hgvsp: ENSP00000413854.1:p.Phe56Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.247T>G
  hgvsp: ENSP00000384099.1:p.Phe83Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.793T>G
  hgvsp: ENSP00000385048.3:p.Phe265Val
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.793T>G
  hgvsp: ENSP00000385727.1:p.Phe265Val
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe265Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-66386028-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386028
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386028
    reference: chr 5
allele count: 1
allele frequency: 8.900281248887465e-6
allele num: 112356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.235A>G
  hgvsp: ENSP00000421739.1:p.Ser79Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.235A>G
  hgvsp: ENSP00000384313.1:p.Ser79Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.175A>G
  hgvsp: ENSP00000413854.1:p.Ser59Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.256A>G
  hgvsp: ENSP00000384099.1:p.Ser86Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.802A>G
  hgvsp: ENSP00000385048.3:p.Ser268Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.220A>G
  hgvsp: ENSP00000392478.1:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.802A>G
  hgvsp: ENSP00000385727.1:p.Ser268Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.220A>G
  hgvsp: ENSP00000398694.1:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.220A>G
  hgvsp: ENSP00000261569.7:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4983
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser268Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

5-66386030-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386030
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386030
    reference: chr 5
allele count: 1
allele frequency: 8.902499821950003e-6
allele num: 112328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.237T>C
  hgvsp: ENST00000403666.1:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.804T>C
  hgvsp: ENST00000403625.2:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000413854
  ensembl transcript: ENST00000432426
  gene symbol: MAST4
  hgvsc: ENST00000432426.1:c.177T>C
  hgvsp: ENST00000432426.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.258T>C
  hgvsp: ENST00000405643.1:c.258T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.237T>C
  hgvsp: ENST00000490016.2:c.237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.804T>C
  hgvsp: ENST00000404260.3:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.222T>C
  hgvsp: ENST00000436277.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.222T>C
  hgvsp: ENST00000447738.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.222T>C
  hgvsp: ENST00000261569.7:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser268Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

5-66386046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386046
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386046
    reference: chr 5
allele count: 1
allele frequency: 8.978756262682494e-6
allele num: 111374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.238T>C
  hgvsp: ENSP00000392478.1:p.Ser80Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.238T>C
  hgvsp: ENSP00000398694.1:p.Ser80Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.253T>C
  hgvsp: ENSP00000384313.1:p.Ser85Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.820T>C
  hgvsp: ENSP00000385727.1:p.Ser274Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.238T>C
  hgvsp: ENSP00000261569.7:p.Ser80Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.820T>C
  hgvsp: ENSP00000385048.3:p.Ser274Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.253T>C
  hgvsp: ENSP00000421739.1:p.Ser85Pro
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.274T>C
  hgvsp: ENSP00000384099.1:p.Ser92Pro
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33531
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser274Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-66386048-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386048
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386048
    reference: chr 5
allele count: 2
allele frequency: 1.803361465772199e-5
allele num: 110904
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.822A>G
  hgvsp: ENST00000403625.2:c.822A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.240A>G
  hgvsp: ENST00000447738.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.822A>G
  hgvsp: ENST00000404260.3:c.822A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.276A>G
  hgvsp: ENST00000405643.1:c.276A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.255A>G
  hgvsp: ENST00000403666.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.255A>G
  hgvsp: ENST00000490016.2:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.240A>G
  hgvsp: ENST00000436277.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.240A>G
  hgvsp: ENST00000261569.7:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser274Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

5-66386070-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386070
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386070
    reference: chr 5
allele count: 13
allele frequency: 1.221712653183971e-4
allele num: 106408
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+11T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+11T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22756
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14284
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

5-66386072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386072
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386072
    reference: chr 5
allele count: 1
allele frequency: 9.434140266797487e-6
allele num: 105998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+13T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+13T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

5-66386090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386090
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386090
    reference: chr 5
allele count: 1
allele frequency: 9.914340101522842e-6
allele num: 100864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+31G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+31G>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5347
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19498
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4701
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-66386092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386092
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386092
    reference: chr 5
allele count: 1
allele frequency: 9.96551930321089e-6
allele num: 100346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+33C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+33C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7226
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

5-66386096-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386096
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386096
    reference: chr 5
allele count: 2
allele frequency: 2.025562600012153e-5
allele num: 98738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+37T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+37T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10940
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4702
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5550
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

5-66386097-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386097
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386097
    reference: chr 5
allele count: 1
allele frequency: 1.015971065144065e-5
allele num: 98428
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+38A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+38A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

5-66386099-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386099
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386099
    reference: chr 5
allele count: 1
allele frequency: 1.032737787875658e-5
allele num: 96830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+40A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+40A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20511
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11828
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7950
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

5-66386099-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386099
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386098
    reference: chr 5
allele count: 1
allele frequency: 1.032737787875658e-5
allele num: 96830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+41delG
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+41delG
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: AG
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

5-66386102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386102
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386102
    reference: chr 5
allele count: 2
allele frequency: 2.096743756945464e-5
allele num: 95386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+43G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+43G>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5278
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7932
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4698
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

5-66386109-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66386109
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66386109
    reference: chr 5
allele count: 3
allele frequency: 3.367759317467445e-5
allele num: 89080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.266+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.266+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.251+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.833+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.251+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.287+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.251+50A>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.833+50A>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6681
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11971
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

5-66389414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389414
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389414
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 20252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-2011G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-2002G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-2011G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-2011G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-2011G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-571G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-2011G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-2011G>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18477
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6141
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20897
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11103
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

5-66389426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389426
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389426
    reference: chr 5
allele count: 1
allele frequency: 4.965243296921549e-5
allele num: 20140
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1999G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1990G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-559G>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25833
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22189
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14012
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3717
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

5-66389470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389470
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389470
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1955G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1955G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1955G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1946G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1955G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1955G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-515G>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1955G>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25391
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24309
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

5-66389476-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389476
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389476
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-509T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1949T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1949T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1949T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1940T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1949T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1949T>A
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1949T>A
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25918
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24848
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

5-66389479-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389479
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389479
    reference: chr 5
allele count: 1
allele frequency: 5.091131249363608e-5
allele num: 19642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1937G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1946G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1946G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1946G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1946G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1946G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-506G>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1946G>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25092
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

5-66389485-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389485
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389485
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-500G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1940G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1940G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1940G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1940G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1931G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1940G>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1940G>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27042
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12498
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

5-66389488-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389488
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389488
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1928C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1937C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-497C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17090
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25754
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

5-66389497-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389497
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389497
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1928A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-488A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1928A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1919A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1928A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1928A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1928A>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1928A>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16295
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11614
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26134
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

5-66389503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389503
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389503
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1922C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1922C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-482C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1913C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1922C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1922C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1922C>T
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1922C>T
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16022
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27710
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10061
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-66389515-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389515
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389515
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 18638
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-470T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1910T>C
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1901T>C
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16190
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

5-66389935-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389935
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389935
    reference: chr 5
allele count: 7
allele frequency: 6.402048655569782e-5
allele num: 109340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1481C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1490C>G
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-50C>G
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10746
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11114
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2819
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

5-66389938-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389938
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389939
    reference: chr 5
allele count: 214
allele frequency: 2.039532622991442e-3
allele num: 104926
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1470dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1479dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1479dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1479dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1479dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-39dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1479dupT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1479dupT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 13880
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 2.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4306
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 2
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

5-66389938-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389938
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389937
    reference: chr 5
allele count: 17
allele frequency: 1.62018946686236e-4
allele num: 104926
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385727
  ensembl transcript: ENST00000403625
  gene symbol: MAST4
  hgvsc: ENST00000403625.2:c.834-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000385048
  ensembl transcript: ENST00000404260
  gene symbol: MAST4
  hgvsc: ENST00000404260.3:c.834-1470delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000398694
  ensembl transcript: ENST00000447738
  gene symbol: MAST4
  hgvsc: ENST00000447738.1:c.252-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000392478
  ensembl transcript: ENST00000436277
  gene symbol: MAST4
  hgvsc: ENST00000436277.1:c.252-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000261569
  ensembl transcript: ENST00000261569
  gene symbol: MAST4
  hgvsc: ENST00000261569.7:c.252-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000421739
  ensembl transcript: ENST00000490016
  gene symbol: MAST4
  hgvsc: ENST00000490016.2:c.267-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384313
  ensembl transcript: ENST00000403666
  gene symbol: MAST4
  hgvsc: ENST00000403666.1:c.267-1479delT
  variant of: http://identifiers.org/hgnc/19037
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000069020
  ensembl protein: ENSP00000384099
  ensembl transcript: ENST00000405643
  gene symbol: MAST4
  hgvsc: ENST00000405643.1:c.288-39delT
  variant of: http://identifiers.org/hgnc/19037
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13880
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5804
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.25e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: CT
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-66389938-CTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66389938
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 66389934
    reference: chr 5
allele count: 1
allele frequency: 9.530526275660943e-6
allele num: 104926
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4306
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3943
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5804
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.287001287001287e-4
  allele num: 7770
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6324
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7964
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 790
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: CTTTT
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1169
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20768
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2372
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.872659176029963e-3
allele num: 1068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.037293039704228e-5
allele num: 12442
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 2.925e0

DP
type: SiteQuality
SIO_000300: 5.78394e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 2.094e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7507
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.710508656556167e-5
allele num: 14902
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.133e0

DP
type: SiteQuality
SIO_000300: 6.23063e5

QD
type: SiteQuality
SIO_000300: 1.523e1

GenotypeQuality
all individuals: 358
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.460783046905285e-5
allele num: 15478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1376
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.102e1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.65219e5

GenotypeQuality
all individuals: 299
bin: 7.25e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 18

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: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 7.681474843169889e-4
allele num: 15622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.425083526085839e-4
allele num: 7782
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.395e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.264e0

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.7536e5

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2014
bin: 3.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3340
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 6.88360450563204e-3
allele num: 1598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

QD
type: SiteQuality
SIO_000300: 1.426e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 4.781e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 7.26759e5

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 204
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

QD
type: SiteQuality
SIO_000300: 1.557e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

DP
type: SiteQuality
SIO_000300: 7.36009e5

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 3.481894150417827e-4
allele num: 17232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

QD
type: SiteQuality
SIO_000300: 1.557e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.36009e5

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.15606936416185e-4
allele num: 17300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3384
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.73e0

FS
type: SiteQuality
SIO_000300: 1.0938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 6.051e1

DP
type: SiteQuality
SIO_000300: 7.42635e5

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8590
bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1939
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.87757909215956e-4
allele num: 1454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2584
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 6.051e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 1.0938e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

DP
type: SiteQuality
SIO_000300: 7.42635e5

QD
type: SiteQuality
SIO_000300: 7.73e0

GenotypeQuality
all individuals: 894
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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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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GenotypeQuality
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GenotypeQuality
all individuals: 342
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1934
bin: 2.75e1
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GenotypeQuality
all individuals: 314
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GenotypeQuality
all individuals: 326
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1860
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1780
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.186721991701245e-5
allele num: 19280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.031e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
SIO_000300: 2.307e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 7.88432e5

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: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.185677021579322e-4
allele num: 8434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2098
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.222e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

QD
type: SiteQuality
SIO_000300: 1.19e1

DP
type: SiteQuality
SIO_000300: 8.11929e5

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22744
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.863e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 2.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 8.42243e5

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: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.776149837625557e-5
allele num: 26482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.99341e5

MQRankSum
type: SiteQuality
SIO_000300: -1.281e0

FS
type: SiteQuality
SIO_000300: 2.735e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -7.684e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

GenotypeQuality
all individuals: 309
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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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bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4116
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36184
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.153316106804479e-4
allele num: 4644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.52e1

DP
type: SiteQuality
SIO_000300: 1.024265e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.006e0

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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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.228e-1

ClippingRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

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

South Asian
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allele count: 2
allele frequency: 1.840264998159735e-4
allele num: 10868
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.577287066246057e-3
allele num: 634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6650
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 1.200840588411888e-3
allele num: 6662
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.408222786715589e-5
allele num: 42516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 1.039e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.109749e6

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.174574870612795e-5
allele num: 45986
num of homozygotes: 0

South Asian
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DP
type: SiteQuality
SIO_000300: 1.155043e6

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5244
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.30718954248366e-4
allele num: 7650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12024
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

QD
type: SiteQuality
SIO_000300: 4.79e0

VQSLOD
type: SiteQuality
SIO_000300: -6.073e-1

DP
type: SiteQuality
SIO_000300: 1.224007e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.816e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.005000000000001e0

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 432
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.278118609406953e-4
allele num: 7824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52202
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: 0
allele frequency: 0.0e0
allele num: 12274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6986
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

DP
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SIO_000300: 1.239094e6

FS
type: SiteQuality
SIO_000300: 1.281e0

QD
type: SiteQuality
SIO_000300: 1.238e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

GenotypeQuality
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bin: 2.5e0
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: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.87336080929187e-4
allele num: 5338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.931247585940517e-5
allele num: 51780
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.87e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

DP
type: SiteQuality
SIO_000300: 1.224448e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.451e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 7.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 7.0e0

GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.446340757882557e-4
allele num: 6914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.928417155199013e-5
allele num: 51856
num of homozygotes: 0

Latino
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: 7772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12184
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 7.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.377e-1

DP
type: SiteQuality
SIO_000300: 1.225821e6

QD
type: SiteQuality
SIO_000300: 6.3e0

GenotypeQuality
all individuals: 561
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5302
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.471020888496617e-4
allele num: 6798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.749e0

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.19e0

QD
type: SiteQuality
SIO_000300: 1.215e1

FS
type: SiteQuality
SIO_000300: 7.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 1.201101e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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bin: 2.75e1
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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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50204
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.317870321560359e-4
allele num: 7588
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.234e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.0492e1

QD
type: SiteQuality
SIO_000300: 1.459e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.170697e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.81e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49674
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.326259946949602e-4
allele num: 7540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.88e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.11e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.894e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.044e0

DP
type: SiteQuality
SIO_000300: 1.152065e6

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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.576292559899117e-4
allele num: 6344
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48344
num of homozygotes: 0

European (Finnish)
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allele count: 0
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allele num: 5086
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.105e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.779e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.11042e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

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

Latino
type: Population
allele count: 1
allele frequency: 1.288327750579748e-4
allele num: 7762
num of homozygotes: 0

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

Other
type: Population
allele count: 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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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48006
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.589825119236884e-3
allele num: 6290
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 1.329e0

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.097056e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

QD
type: SiteQuality
SIO_000300: 9.18e0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 5.75e1
variant carriers: 0

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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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.75e1
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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 9.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.981767736821245e-4
allele num: 5046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.315107126320664e-4
allele num: 47514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 4.133e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

DP
type: SiteQuality
SIO_000300: 1.083089e6

GenotypeQuality
all individuals: 594
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.200123206899586e-5
allele num: 45452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.106e0

VQSLOD
type: SiteQuality
SIO_000300: -3.556e-1

FS
type: SiteQuality
SIO_000300: 2.231e0

QD
type: SiteQuality
SIO_000300: 1.233e1

DP
type: SiteQuality
SIO_000300: 1.015748e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.877e0

GenotypeQuality
all individuals: 1070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
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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: 17

GenotypeQuality
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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
all individuals: 311
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32614
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

East Asian
type: Population
allele count: 16
allele frequency: 3.068661296509398e-3
allele num: 5214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41492
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 9.12663e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.217e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3156
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7928
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.490908185124296e-5
allele num: 40146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.486e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

DP
type: SiteQuality
SIO_000300: 8.89399e5

MQRankSum
type: SiteQuality
SIO_000300: 2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

FS
type: SiteQuality
SIO_000300: 3.264e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.435e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
all individuals: 401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5511
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GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 311
bin: 9.25e1
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GenotypeQuality
all individuals: 7590
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 3553
bin: 9.75e1
variant carriers: 118

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 6.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.426737494466578e-4
allele num: 4518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.162555344718533e-4
allele num: 6324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 72
allele frequency: 1.807228915662651e-3
allele num: 39840
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 9.99000999000999e-4
allele num: 6006
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 2.150336574420344e-3
allele num: 10696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.977e0

DP
type: SiteQuality
SIO_000300: 8.82439e5

FS
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 5.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
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GenotypeQuality
all individuals: 90
bin: 4.75e1
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GenotypeQuality
all individuals: 310
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variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 2.5e0
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GenotypeQuality
all individuals: 1057
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31490
bin: 2.25e1
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GenotypeQuality
all individuals: 1290
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 3230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.553365335512205e-5
allele num: 39164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.71042e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 7.152e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.422e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3558
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variant carriers: 0

GenotypeQuality
all individuals: 2791
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GenotypeQuality
all individuals: 1176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 321
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GenotypeQuality
all individuals: 310
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variant carriers: 0

GenotypeQuality
all individuals: 4595
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.108486167236556e-5
allele num: 32170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.00542e5

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 3.383e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.022e0

FS
type: SiteQuality
SIO_000300: 3.0343e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 639
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43952
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.737921445950643e-4
allele num: 5754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

FS
type: SiteQuality
SIO_000300: 1.119e0

QD
type: SiteQuality
SIO_000300: 1.355e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.024e0

DP
type: SiteQuality
SIO_000300: 1.122511e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 8099
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variant carriers: 0

GenotypeQuality
all individuals: 630
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GenotypeQuality
all individuals: 753
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GenotypeQuality
all individuals: 5115
bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4703
bin: 9.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.286027798098025e-5
allele num: 43744
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

QD
type: SiteQuality
SIO_000300: 9.83e0

DP
type: SiteQuality
SIO_000300: 1.124074e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.041e-1

FS
type: SiteQuality
SIO_000300: 8.016e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.69664065151001e-4
allele num: 5894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.445e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.174096e6

FS
type: SiteQuality
SIO_000300: 6.698e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.220840365994492e-5
allele num: 45028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7350
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

VQSLOD
type: SiteQuality
SIO_000300: -3.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 5.59e0

DP
type: SiteQuality
SIO_000300: 1.186887e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5276
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46454
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.69606512890095e-4
allele num: 11792
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.088e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

FS
type: SiteQuality
SIO_000300: 1.544e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

QD
type: SiteQuality
SIO_000300: 1.501e1

DP
type: SiteQuality
SIO_000300: 1.243792e6

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.278772378516624e-4
allele num: 7820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.261516e6

FS
type: SiteQuality
SIO_000300: 4.151e0

QD
type: SiteQuality
SIO_000300: 1.01e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.567e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.929310078715851e-5
allele num: 51832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.859e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.391129e6

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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.192748091603053e-4
allele num: 8384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.819902453228507e-5
allele num: 54948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12784
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.38e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.115e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 1.451065e6

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608699848782214e-5
allele num: 62162
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
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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10854
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.994963626189144e-5
allele num: 14296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.422e0

DP
type: SiteQuality
SIO_000300: 1.593966e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.629e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

QD
type: SiteQuality
SIO_000300: 8.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.223390518354546e-5
allele num: 10842
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

FS
type: SiteQuality
SIO_000300: 1.325e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.593423e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610046691354049e-5
allele num: 62110
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.029e-1

DP
type: SiteQuality
SIO_000300: 1.573818e6

QD
type: SiteQuality
SIO_000300: 7.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.885e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.199252254233561e-4
allele num: 9094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.469e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 1.563768e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 974
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

GenotypeQuality
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GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.556016597510373e-3
allele num: 7712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.694800352518473e-5
allele num: 59004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

FS
type: SiteQuality
SIO_000300: 2.938e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.437485e6

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701027420562019e-5
allele num: 58788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8852
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.905e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.204e0

FS
type: SiteQuality
SIO_000300: 1.405e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.344e0

VQSLOD
type: SiteQuality
SIO_000300: -3.553e0

QD
type: SiteQuality
SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 1.420915e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

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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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.398601398601399e-4
allele num: 7150
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.305e0

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.639e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.46e-1

DP
type: SiteQuality
SIO_000300: 1.256732e6

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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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.802776275464215e-5
allele num: 55470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7120
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.782e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.24951e6

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.59e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.263e1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.669455452810803e-5
allele num: 54504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

QD
type: SiteQuality
SIO_000300: 1.079e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: 6.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

DP
type: SiteQuality
SIO_000300: 1.22823e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1101
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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: 7792
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GenotypeQuality
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GenotypeQuality
all individuals: 895
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variant carriers: 0

GenotypeQuality
all individuals: 564
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5638
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.62660158633313e-5
allele num: 13112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

FS
type: SiteQuality
SIO_000300: 2.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

DP
type: SiteQuality
SIO_000300: 1.22363e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.061e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

QD
type: SiteQuality
SIO_000300: 1.478e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.461133839859731e-4
allele num: 6844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

FS
type: SiteQuality
SIO_000300: 2.945e0

QD
type: SiteQuality
SIO_000300: 1.611e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

DP
type: SiteQuality
SIO_000300: 1.213149e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.874203463528001e-5
allele num: 53356
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.945e0

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

QD
type: SiteQuality
SIO_000300: 1.611e1

DP
type: SiteQuality
SIO_000300: 1.213149e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52520
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.963841138114997e-4
allele num: 6748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5456
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e0

MQ
type: SiteQuality
SIO_000300: 6.051e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.247e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 1.207842e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 1916
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variant carriers: 0

GenotypeQuality
all individuals: 5507
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5160
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.854368932038835e-4
allele num: 6180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12360
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.656e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 6.5e0

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 1.199715e6

GenotypeQuality
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bin: 2.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 592
bin: 7.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 966
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.15e0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.68e0

VQSLOD
type: SiteQuality
SIO_000300: -1.805e0

DP
type: SiteQuality
SIO_000300: 5.06461e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.68e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 542
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.348435814455232e-4
allele num: 7416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.378e-1

DP
type: SiteQuality
SIO_000300: 5.14126e5

FS
type: SiteQuality
SIO_000300: 7.532e0

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.55e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 1382
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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7286
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 410
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: 7236
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

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

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1728
num of homozygotes: 0

South Asian
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allele num: 7888
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7164
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.006e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.718e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -4.9e-2

DP
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SIO_000300: 5.13119e5

ReadPosRankSum
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.182e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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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
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.04031e5

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.15e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 1.511e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1344
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.652e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.08e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 5.04891e5

FS
type: SiteQuality
SIO_000300: 6.854e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.521e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.307e0

QD
type: SiteQuality
SIO_000300: 1.114e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.25e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 4.96272e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6792
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1300
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 4.89523e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.42e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
all individuals: 4373
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 590
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.83213e5

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.593e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.76e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.171587333467229e-4
allele num: 59748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6402
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10904
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.419e1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.442874e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 192

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 19
allele frequency: 1.843944099378882e-3
allele num: 10304
num of homozygotes: 0

African
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allele count: 163
allele frequency: 2.097812097812098e-2
allele num: 7770
num of homozygotes: 2

European (Non-Finnish)
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allele count: 26
allele frequency: 4.53530560982417e-4
allele num: 57328
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.162555344718533e-4
allele num: 6324
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.768932576491763e-4
allele num: 14446
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.453912e6

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 814
bin: 1.75e1
variant carriers: 5

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.442087636059168e-4
allele num: 57328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.076699432368822e-4
allele num: 14446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.69e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

DP
type: SiteQuality
SIO_000300: 1.453912e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

DP
type: SiteQuality
SIO_000300: 1.453912e6