22-37420855-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420855
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420855
    reference: chr 22
allele count: 1
allele frequency: 1.125847200018014e-5
allele num: 88822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.874A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+4A>G
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2138
  bin: 6.75e1
  variant carriers: 0
hgvs: c.655+4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

22-37420856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420856
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420856
    reference: chr 22
allele count: 2
allele frequency: 2.256674113691242e-5
allele num: 88626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+5C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.875C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
hgvs: c.655+5C>T
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/22-37420858-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420858
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420858
    reference: chr 22
allele count: 1
allele frequency: 1.147552271005944e-5
allele num: 87142
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.877C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+7C>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16869
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
hgvs: c.655+7C>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-37420858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420858
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420858
    reference: chr 22
allele count: 2
allele frequency: 2.295104542011889e-5
allele num: 87142
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.877C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+7C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12777
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.25e1
  variant carriers: 0
hgvs: c.655+7C>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

22-37420859-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420859
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420859
    reference: chr 22
allele count: 2
allele frequency: 2.334321529447466e-5
allele num: 85678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.878G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+8G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+8G>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16010
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
hgvs: c.655+8G>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

22-37420861-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420861
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420861
    reference: chr 22
allele count: 26
allele frequency: 3.033838973162194e-4
allele num: 85700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.880G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+10G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16166
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum

22-37420863-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420863
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420863
    reference: chr 22
allele count: 1
allele frequency: 1.19465749169713e-5
allele num: 83706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.882G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+12G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+12G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24643
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

22-37420866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420866
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420866
    reference: chr 22
allele count: 1
allele frequency: 1.243533625149224e-5
allele num: 80416
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.885G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+15G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4047
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

22-37420867-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420867
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420867
    reference: chr 22
allele count: 5
allele frequency: 6.223240067708852e-5
allele num: 80344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.886G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+16G>C
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15331
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12721
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17804
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2578
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-37420870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420870
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420870
    reference: chr 22
allele count: 20
allele frequency: 2.623914355435438e-4
allele num: 76222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.889G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+19G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17481
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29090
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

22-37420886-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420886
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420886
    reference: chr 22
allele count: 1
allele frequency: 1.666277868497351e-5
allele num: 60014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.905G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+35G>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2505
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8768
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-37420890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420890
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420890
    reference: chr 22
allele count: 6237
allele frequency: 1.132558561830398e-1
allele num: 55070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+39C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.909C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 2.5e0
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 20598
  bin: 7.5e0
  variant carriers: 1345
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 16366
  bin: 1.25e1
  variant carriers: 2350
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 1.75e1
  variant carriers: 1848
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 2.25e1
  variant carriers: 755
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.75e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 27435
  bin: 2.25e1
  variant carriers: 122
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 1.75e1
  variant carriers: 137
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 168
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 173
genotype quality: GenotypeQuality
  all individuals: 6150
  bin: 6.25e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 6.75e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 126
genotype quality: GenotypeQuality
  all individuals: 9869
  bin: 7.5e0
  variant carriers: 95
num of homozygotes: 563
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

22-37420906-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420906
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420906
    reference: chr 22
allele count: 2
allele frequency: 4.559963520291838e-5
allele num: 43860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.925A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+55A>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20475
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6043
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

22-37420912-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420912
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420912
    reference: chr 22
allele count: 1
allele frequency: 2.623157232044489e-5
allele num: 38122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.931G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+61G>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

22-37420913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420913
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420913
    reference: chr 22
allele count: 2
allele frequency: 5.426230397742688e-5
allele num: 36858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.932C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+62C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16944
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23354
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

22-37420926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420926
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420926
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 20848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.945C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+75C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10271
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33099
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9019
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

22-37420926-CTTTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420926
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420921
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 20848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.949_953delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+79_655+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+79_595+83delCTTTT
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10271
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33099
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: CTTTCT
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

22-37420929-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420929
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420928
    reference: chr 22
allele count: 2
allele frequency: 1.077702338614075e-4
allele num: 18558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.949delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+79delC
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33591
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TC
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

22-37420944-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420944
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420944
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 15700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.963A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+93A>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31810
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31210
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

22-37420959-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420959
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420959
    reference: chr 22
allele count: 3
allele frequency: 1.960528035550908e-4
allele num: 15302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.978A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+108A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.596-84A>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25839
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5961
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

22-37420963-CCTTTCCTTTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420963
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420951
    reference: chr 22
allele count: 3
allele frequency: 1.965151316651382e-4
allele num: 15266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22912
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: CCTTTCCTTTTTT
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-37420968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420968
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420968
    reference: chr 22
allele count: 1
allele frequency: 6.579813133307015e-5
allele num: 15198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.987C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+117C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+117C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+117C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+117C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+117C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.596-75C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+117C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

22-37420969-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37420969
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37420968
    reference: chr 22
allele count: 1
allele frequency: 6.597176408497163e-5
allele num: 15158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.596-68delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+124delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+124delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.994delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+124delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+124delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+124delT
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+124delT
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: CT
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

22-37421008-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37421008
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37421007
    reference: chr 22
allele count: 3
allele frequency: 2.001868410516482e-4
allele num: 14986
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+162delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+162delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.596-30delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+162delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+162delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+162delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.1032delC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+162delC
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: TC
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

22-37421057-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37421057
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37421057
    reference: chr 22
allele count: 3
allele frequency: 1.981767736821245e-4
allele num: 15138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+206G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+206G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+206G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+206G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+206G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.1076G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.610G>T
  hgvsp: ENSP00000385062.1:p.Ala204Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+206G>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala204Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

22-37421092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37421092
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37421092
    reference: chr 22
allele count: 1
allele frequency: 6.390593047034765e-5
allele num: 15648
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.645A>G
  hgvsp: ENST00000404393.1:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+241A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+241A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+241A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+241A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.1111A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+241A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+241A>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser215Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-37421094-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37421094
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37421094
    reference: chr 22
allele count: 4
allele frequency: 2.552974214960429e-4
allele num: 15668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.1113T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+243T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+243T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.647T>G
  hgvsp: ENSP00000385062.1:p.Leu216Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+243T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+243T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+243T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+243T>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6197
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu216Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ

22-37421166-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37421166
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37421166
    reference: chr 22
allele count: 1
allele frequency: 6.202704379109291e-5
allele num: 16122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.1185G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.595+315G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.595+315G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*44G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.595+315G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.595+315G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.655+315G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.595+315G>C
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
hgvs: c.*44G>C
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-37425198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425198
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425198
    reference: chr 22
allele count: 2
allele frequency: 2.589533107180775e-5
allele num: 77234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-59C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5217C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-59C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10522
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5539
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

22-37425199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425199
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425199
    reference: chr 22
allele count: 1
allele frequency: 1.292256797270754e-5
allele num: 77384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5218G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-58G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-58G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18390
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22500
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

22-37425201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425201
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425201
    reference: chr 22
allele count: 13095
allele frequency: 1.662899375222228e-1
allele num: 78748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5220G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-56G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-56G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.5e0
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.25e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 1.75e1
  variant carriers: 3598
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 17463
  bin: 7.5e0
  variant carriers: 3511
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 2.75e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 22484
  bin: 1.25e1
  variant carriers: 6260
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.25e1
  variant carriers: 1242
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 11004
  bin: 2.25e1
  variant carriers: 209
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 6.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.75e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 6.25e1
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 4714
  bin: 2.75e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 7.5e0
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 2141
  bin: 2.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 1.75e1
  variant carriers: 146
num of homozygotes: 1159
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

22-37425202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425202
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425202
    reference: chr 22
allele count: 13298
allele frequency: 1.67793872709837e-1
allele num: 79252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-55G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5221G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 2.25e1
  variant carriers: 1314
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 1.75e1
  variant carriers: 3723
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.75e1
  variant carriers: 462
genotype depth: GenotypeDepth
  all individuals: 22420
  bin: 1.25e1
  variant carriers: 6193
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.5e0
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17277
  bin: 7.5e0
  variant carriers: 3339
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 5.25e1
  variant carriers: 162
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 3.75e1
  variant carriers: 286
genotype quality: GenotypeQuality
  all individuals: 13410
  bin: 9.75e1
  variant carriers: 13294
genotype quality: GenotypeQuality
  all individuals: 4727
  bin: 2.75e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 212
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 1.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.25e1
  variant carriers: 36
num of homozygotes: 1176
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-37425203-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425203
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425203
    reference: chr 22
allele count: 1
allele frequency: 1.246136975376333e-5
allele num: 80248
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-54T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5222T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-54T>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16967
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/22-37425206-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425206
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425205
    reference: chr 22
allele count: 1
allele frequency: 1.226903540843619e-5
allele num: 81506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5226delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-50delA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-50delA
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: CA
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

22-37425216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425216
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425216
    reference: chr 22
allele count: 1
allele frequency: 1.186070784704431e-5
allele num: 84312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5235A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-41A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-41A>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8562
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

22-37425222-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425222
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425222
    reference: chr 22
allele count: 1
allele frequency: 1.160820003250296e-5
allele num: 86146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5241C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-35C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-35C>G
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17830
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

22-37425237-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425237
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425237
    reference: chr 22
allele count: 1
allele frequency: 1.017231908530507e-5
allele num: 98306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5256T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-20T>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-20T>A
  variant of: http://identifiers.org/hgnc/7223
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-37425251-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425251
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425251
    reference: chr 22
allele count: 1
allele frequency: 9.134088417975885e-6
allele num: 109480
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-6C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5270C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-6C>G
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
hgvs: c.656-6C>G
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: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS

22-37425253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425253
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425253
    reference: chr 22
allele count: 1
allele frequency: 9.04224537037037e-6
allele num: 110592
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596-4G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5272G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
hgvs: c.656-4G>A
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-37425257-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425257
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425257
    reference: chr 22
allele count: 1
allele frequency: 8.919015340706385e-6
allele num: 112120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.596G>A
  hgvsp: ENSP00000342333.3:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.596G>A
  hgvsp: ENSP00000411719.2:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.596G>A
  hgvsp: ENSP00000380402.2:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.596G>A
  hgvsp: ENSP00000383950.3:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.656G>A
  hgvsp: ENSP00000380318.1:p.Gly219Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.596G>A
  hgvsp: ENSP00000384812.3:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5276G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9145
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly219Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

22-37425281-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425281
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425281
    reference: chr 22
allele count: 1
allele frequency: 8.498631720293032e-6
allele num: 117666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.620G>C
  hgvsp: ENSP00000342333.3:p.Gly207Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5300G>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.620G>C
  hgvsp: ENSP00000380402.2:p.Gly207Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.680G>C
  hgvsp: ENSP00000380318.1:p.Gly227Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.620G>C
  hgvsp: ENSP00000384812.3:p.Gly207Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.620G>C
  hgvsp: ENSP00000383950.3:p.Gly207Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.620G>C
  hgvsp: ENSP00000411719.2:p.Gly207Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11659
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly227Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-37425285-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425285
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425285
    reference: chr 22
allele count: 7
allele frequency: 5.926678520023707e-5
allele num: 118110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.624C>T
  hgvsp: ENST00000341116.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.684C>T
  hgvsp: ENST00000397129.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.624C>T
  hgvsp: ENST00000401419.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.624C>T
  hgvsp: ENST00000397225.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.624C>T
  hgvsp: ENST00000429360.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5304C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.624C>T
  hgvsp: ENST00000404802.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*75C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43388
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr228Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

22-37425286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425286
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425286
    reference: chr 22
allele count: 4
allele frequency: 3.380091262464087e-5
allele num: 118340
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.685G>A
  hgvsp: ENSP00000380318.1:p.Val229Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.625G>A
  hgvsp: ENSP00000384812.3:p.Val209Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.625G>A
  hgvsp: ENSP00000342333.3:p.Val209Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.625G>A
  hgvsp: ENSP00000383950.3:p.Val209Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.625G>A
  hgvsp: ENSP00000411719.2:p.Val209Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5305G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*76G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.625G>A
  hgvsp: ENSP00000380402.2:p.Val209Met
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3683
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val229Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

22-37425290-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425290
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425290
    reference: chr 22
allele count: 3
allele frequency: 2.523171121465458e-5
allele num: 118898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.629A>T
  hgvsp: ENSP00000383950.3:p.Asn210Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.629A>T
  hgvsp: ENSP00000342333.3:p.Asn210Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.629A>T
  hgvsp: ENSP00000384812.3:p.Asn210Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.629A>T
  hgvsp: ENSP00000411719.2:p.Asn210Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.689A>T
  hgvsp: ENSP00000380318.1:p.Asn230Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.629A>T
  hgvsp: ENSP00000380402.2:p.Asn210Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5309A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*80A>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn230Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

22-37425292-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425292
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425292
    reference: chr 22
allele count: 1
allele frequency: 8.398562166157153e-6
allele num: 119068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.631A>T
  hgvsp: ENSP00000380402.2:p.Ile211Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.691A>T
  hgvsp: ENSP00000380318.1:p.Ile231Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*82A>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.631A>T
  hgvsp: ENSP00000342333.3:p.Ile211Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.631A>T
  hgvsp: ENSP00000411719.2:p.Ile211Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.631A>T
  hgvsp: ENSP00000384812.3:p.Ile211Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.631A>T
  hgvsp: ENSP00000383950.3:p.Ile211Phe
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5311A>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile231Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

22-37425307-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425307
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425307
    reference: chr 22
allele count: 1
allele frequency: 8.344041519950603e-6
allele num: 119846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.646T>G
  hgvsp: ENSP00000411719.2:p.Phe216Val
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.646T>G
  hgvsp: ENSP00000383950.3:p.Phe216Val
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.646T>G
  hgvsp: ENSP00000380402.2:p.Phe216Val
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.646T>G
  hgvsp: ENSP00000384812.3:p.Phe216Val
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.706T>G
  hgvsp: ENSP00000380318.1:p.Phe236Val
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5326T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*97T>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.646T>G
  hgvsp: ENSP00000342333.3:p.Phe216Val
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe236Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

22-37425323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425323
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425323
    reference: chr 22
allele count: 2
allele frequency: 1.660798511924533e-5
allele num: 120424
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.722G>A
  hgvsp: ENSP00000380318.1:p.Gly241Glu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.662G>A
  hgvsp: ENSP00000411719.2:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5342G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.662G>A
  hgvsp: ENSP00000383950.3:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.662G>A
  hgvsp: ENSP00000342333.3:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*113G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.662G>A
  hgvsp: ENSP00000380402.2:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.662G>A
  hgvsp: ENSP00000384812.3:p.Gly221Glu
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly241Glu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

22-37425324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425324
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425324
    reference: chr 22
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.663G>A
  hgvsp: ENST00000341116.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.663G>A
  hgvsp: ENST00000404802.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.663G>A
  hgvsp: ENST00000429360.2:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.663G>A
  hgvsp: ENST00000397225.2:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.663G>A
  hgvsp: ENST00000401419.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.723G>A
  hgvsp: ENST00000397129.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5343G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly241Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ

22-37425326-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425326
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425326
    reference: chr 22
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.665T>C
  hgvsp: ENSP00000384812.3:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.725T>C
  hgvsp: ENSP00000380318.1:p.Leu242Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.665T>C
  hgvsp: ENSP00000342333.3:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*116T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.665T>C
  hgvsp: ENSP00000411719.2:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.665T>C
  hgvsp: ENSP00000380402.2:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5345T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.665T>C
  hgvsp: ENSP00000383950.3:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43402
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu242Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

22-37425332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425332
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425332
    reference: chr 22
allele count: 8
allele frequency: 6.630640188310181e-5
allele num: 120652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.671A>G
  hgvsp: ENSP00000411719.2:p.Lys224Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.731A>G
  hgvsp: ENSP00000380318.1:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.671A>G
  hgvsp: ENSP00000342333.3:p.Lys224Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*122A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.671A>G
  hgvsp: ENSP00000384812.3:p.Lys224Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5351A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.671A>G
  hgvsp: ENSP00000383950.3:p.Lys224Arg
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.671A>G
  hgvsp: ENSP00000380402.2:p.Lys224Arg
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys244Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

22-37425347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425347
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425347
    reference: chr 22
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.686T>C
  hgvsp: ENSP00000411719.2:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.746T>C
  hgvsp: ENSP00000380318.1:p.Ile249Thr
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*137T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.686T>C
  hgvsp: ENSP00000380402.2:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.686T>C
  hgvsp: ENSP00000383950.3:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.686T>C
  hgvsp: ENSP00000342333.3:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5366T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.686T>C
  hgvsp: ENSP00000384812.3:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile249Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-37425349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425349
    reference: chr 22
allele count: 4
allele frequency: 3.311367926090268e-5
allele num: 120796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.688C>T
  hgvsp: ENSP00000342333.3:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.688C>T
  hgvsp: ENSP00000384812.3:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.688C>T
  hgvsp: ENSP00000380402.2:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.748C>T
  hgvsp: ENSP00000380318.1:p.Arg250Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.688C>T
  hgvsp: ENSP00000411719.2:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.688C>T
  hgvsp: ENSP00000383950.3:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5368C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53812
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg250Cys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

22-37425350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425350
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425350
    reference: chr 22
allele count: 3
allele frequency: 2.483567064589301e-5
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.689G>A
  hgvsp: ENSP00000384812.3:p.Arg230His
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.689G>A
  hgvsp: ENSP00000383950.3:p.Arg230His
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.689G>A
  hgvsp: ENSP00000411719.2:p.Arg230His
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.749G>A
  hgvsp: ENSP00000380318.1:p.Arg250His
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5369G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.689G>A
  hgvsp: ENSP00000342333.3:p.Arg230His
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.689G>A
  hgvsp: ENSP00000380402.2:p.Arg230His
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43313
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg250His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-37425356-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425356
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425356
    reference: chr 22
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*146T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.695T>C
  hgvsp: ENSP00000342333.3:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5375T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.695T>C
  hgvsp: ENSP00000384812.3:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.695T>C
  hgvsp: ENSP00000411719.2:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.695T>C
  hgvsp: ENSP00000380402.2:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.695T>C
  hgvsp: ENSP00000383950.3:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.755T>C
  hgvsp: ENSP00000380318.1:p.Leu252Pro
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3958
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu252Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

22-37425364-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425364
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425364
    reference: chr 22
allele count: 5
allele frequency: 4.137428836224017e-5
allele num: 120848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.703G>A
  hgvsp: ENSP00000342333.3:p.Glu235Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.703G>A
  hgvsp: ENSP00000384812.3:p.Glu235Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.763G>A
  hgvsp: ENSP00000380318.1:p.Glu255Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.703G>A
  hgvsp: ENSP00000380402.2:p.Glu235Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.703G>A
  hgvsp: ENSP00000411719.2:p.Glu235Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.703G>A
  hgvsp: ENSP00000383950.3:p.Glu235Lys
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5383G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*154G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53962
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu255Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

22-37425364-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425364
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425361
    reference: chr 22
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*159_*161delGAA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.708_710delGAA
  hgvsp: ENSP00000380402.2:p.Lys237del
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.708_710delGAA
  hgvsp: ENSP00000383950.3:p.Lys237del
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.768_770delGAA
  hgvsp: ENSP00000380318.1:p.Lys257del
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.708_710delGAA
  hgvsp: ENSP00000411719.2:p.Lys237del
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.708_710delGAA
  hgvsp: ENSP00000342333.3:p.Lys237del
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5388_5390delGAA
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.708_710delGAA
  hgvsp: ENSP00000384812.3:p.Lys237del
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys257del
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: GAGA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

22-37425373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425373
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425373
    reference: chr 22
allele count: 1
allele frequency: 8.277597510098669e-6
allele num: 120808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.712G>A
  hgvsp: ENSP00000411719.2:p.Val238Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.712G>A
  hgvsp: ENSP00000342333.3:p.Val238Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.712G>A
  hgvsp: ENSP00000380402.2:p.Val238Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.712G>A
  hgvsp: ENSP00000384812.3:p.Val238Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.772G>A
  hgvsp: ENSP00000380318.1:p.Val258Met
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*163G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5392G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.712G>A
  hgvsp: ENSP00000383950.3:p.Val238Met
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val258Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

22-37425377-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425377
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425377
    reference: chr 22
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.776A>G
  hgvsp: ENSP00000380318.1:p.Asp259Gly
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.716A>G
  hgvsp: ENSP00000342333.3:p.Asp239Gly
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.716A>G
  hgvsp: ENSP00000411719.2:p.Asp239Gly
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*167A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.716A>G
  hgvsp: ENSP00000383950.3:p.Asp239Gly
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5396A>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.716A>G
  hgvsp: ENSP00000380402.2:p.Asp239Gly
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.716A>G
  hgvsp: ENSP00000384812.3:p.Asp239Gly
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp259Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

22-37425381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425381
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425381
    reference: chr 22
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.720G>A
  hgvsp: ENST00000404802.3:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.720G>A
  hgvsp: ENST00000397225.2:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.720G>A
  hgvsp: ENST00000429360.2:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5400G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.720G>A
  hgvsp: ENST00000341116.3:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.780G>A
  hgvsp: ENST00000397129.1:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.720G>A
  hgvsp: ENST00000401419.3:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*171G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu260Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

22-37425382-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425382
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425382
    reference: chr 22
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.721T>C
  hgvsp: ENSP00000384812.3:p.Ser241Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.721T>C
  hgvsp: ENSP00000342333.3:p.Ser241Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.721T>C
  hgvsp: ENSP00000380402.2:p.Ser241Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*172T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5401T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.781T>C
  hgvsp: ENSP00000380318.1:p.Ser261Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.721T>C
  hgvsp: ENSP00000383950.3:p.Ser241Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.721T>C
  hgvsp: ENSP00000411719.2:p.Ser241Pro
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser261Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

22-37425382-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425382
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425383
    reference: chr 22
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: TC
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.782dupC
  hgvsp: ENSP00000380318.1:p.Lys262Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.722dupC
  hgvsp: ENSP00000384812.3:p.Lys242Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*173dupC
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.722dupC
  hgvsp: ENSP00000380402.2:p.Lys242Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.722dupC
  hgvsp: ENSP00000383950.3:p.Lys242Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.722dupC
  hgvsp: ENSP00000411719.2:p.Lys242Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.722dupC
  hgvsp: ENSP00000342333.3:p.Lys242Ter
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5402dupC
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys262Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

22-37425394-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425394
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425394
    reference: chr 22
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.733G>T
  hgvsp: ENSP00000384812.3:p.Val245Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5413G>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.733G>T
  hgvsp: ENSP00000411719.2:p.Val245Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.733G>T
  hgvsp: ENSP00000380402.2:p.Val245Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.733G>T
  hgvsp: ENSP00000383950.3:p.Val245Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.733G>T
  hgvsp: ENSP00000342333.3:p.Val245Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.793G>T
  hgvsp: ENSP00000380318.1:p.Val265Leu
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*184G>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val265Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

22-37425395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425395
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425395
    reference: chr 22
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.794T>C
  hgvsp: ENSP00000380318.1:p.Val265Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.734T>C
  hgvsp: ENSP00000380402.2:p.Val245Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.734T>C
  hgvsp: ENSP00000342333.3:p.Val245Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5414T>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.734T>C
  hgvsp: ENSP00000411719.2:p.Val245Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.734T>C
  hgvsp: ENSP00000383950.3:p.Val245Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.734T>C
  hgvsp: ENSP00000384812.3:p.Val245Ala
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*185T>C
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val265Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

22-37425402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425402
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425402
    reference: chr 22
allele count: 3
allele frequency: 2.492025518341308e-5
allele num: 120384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.741G>A
  hgvsp: ENST00000341116.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.741G>A
  hgvsp: ENST00000397225.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.741G>A
  hgvsp: ENST00000404802.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.741G>A
  hgvsp: ENST00000401419.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.801G>A
  hgvsp: ENST00000397129.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5421G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.741G>A
  hgvsp: ENST00000429360.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*192G>A
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr267Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

22-37425415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425415
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425415
    reference: chr 22
allele count: 5
allele frequency: 4.164653750687168e-5
allele num: 120058
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.814G>A
  hgvsp: ENSP00000380318.1:p.Val272Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.754G>A
  hgvsp: ENSP00000383950.3:p.Val252Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.754G>A
  hgvsp: ENSP00000384812.3:p.Val252Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.754G>A
  hgvsp: ENSP00000411719.2:p.Val252Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.754G>A
  hgvsp: ENSP00000342333.3:p.Val252Ile
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5434G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*205G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.754G>A
  hgvsp: ENSP00000380402.2:p.Val252Ile
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42310
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51963
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val272Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-37425428-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425428
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425428
    reference: chr 22
allele count: 2
allele frequency: 1.668613382279326e-5
allele num: 119860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.767A>C
  hgvsp: ENSP00000384812.3:p.His256Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.767A>C
  hgvsp: ENSP00000342333.3:p.His256Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5447A>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.767A>C
  hgvsp: ENSP00000411719.2:p.His256Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.767A>C
  hgvsp: ENSP00000380402.2:p.His256Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*218A>C
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.767A>C
  hgvsp: ENSP00000383950.3:p.His256Pro
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.827A>C
  hgvsp: ENSP00000380318.1:p.His276Pro
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His276Pro
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

22-37425429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425429
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425429
    reference: chr 22
allele count: 13
allele frequency: 1.084743499883181e-4
allele num: 119844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.768C>T
  hgvsp: ENST00000341116.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.768C>T
  hgvsp: ENST00000429360.2:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5448C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.768C>T
  hgvsp: ENST00000404802.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.828C>T
  hgvsp: ENST00000397129.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.768C>T
  hgvsp: ENST00000397225.2:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.768C>T
  hgvsp: ENST00000401419.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His276His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-37425444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425444
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425444
    reference: chr 22
allele count: 2
allele frequency: 1.674116485025028e-5
allele num: 119466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*234C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.843C>T
  hgvsp: ENST00000397129.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.783C>T
  hgvsp: ENST00000404802.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.783C>T
  hgvsp: ENST00000429360.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.783C>T
  hgvsp: ENST00000341116.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5463C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.783C>T
  hgvsp: ENST00000401419.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.783C>T
  hgvsp: ENST00000397225.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala281Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-37425450-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425450
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425450
    reference: chr 22
allele count: 1
allele frequency: 8.386025527061704e-6
allele num: 119246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.789C>G
  hgvsp: ENST00000397225.2:c.789C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.789C>G
  hgvsp: ENST00000429360.2:c.789C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*240C>G
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.789C>G
  hgvsp: ENST00000401419.3:c.789C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.849C>G
  hgvsp: ENST00000397129.1:c.849C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.789C>G
  hgvsp: ENST00000404802.3:c.789C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.789C>G
  hgvsp: ENST00000341116.3:c.789C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5469C>G
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu283Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

22-37425453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425453
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425453
    reference: chr 22
allele count: 5
allele frequency: 4.197588904933006e-5
allele num: 119116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.792C>T
  hgvsp: ENST00000401419.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.792C>T
  hgvsp: ENST00000404802.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.852C>T
  hgvsp: ENST00000397129.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.792C>T
  hgvsp: ENST00000397225.2:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.792C>T
  hgvsp: ENST00000429360.2:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.792C>T
  hgvsp: ENST00000341116.3:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5472C>T
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys284Cys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS

22-37425454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37425454
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 37425454
    reference: chr 22
allele count: 3
allele frequency: 2.519314746388982e-5
allele num: 119080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000342333
  ensembl transcript: ENST00000341116
  gene symbol: MPST
  hgvsc: ENST00000341116.3:c.793G>A
  hgvsp: ENSP00000342333.3:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000385062
  ensembl transcript: ENST00000404393
  gene symbol: MPST
  hgvsc: ENST00000404393.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000128309
  ensembl transcript: ENST00000485587
  gene symbol: MPST
  hgvsc: ENST00000485587.1:n.5473G>A
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380402
  ensembl transcript: ENST00000397225
  gene symbol: MPST
  hgvsc: ENST00000397225.2:c.793G>A
  hgvsp: ENSP00000380402.2:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000384812
  ensembl transcript: ENST00000401419
  gene symbol: MPST
  hgvsc: ENST00000401419.3:c.793G>A
  hgvsp: ENSP00000384812.3:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000380318
  ensembl transcript: ENST00000397129
  gene symbol: MPST
  hgvsc: ENST00000397129.1:c.853G>A
  hgvsp: ENSP00000380318.1:p.Gly285Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000411719
  ensembl transcript: ENST00000429360
  gene symbol: MPST
  hgvsc: ENST00000429360.2:c.793G>A
  hgvsp: ENSP00000411719.2:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/7223
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128309
  ensembl protein: ENSP00000383950
  ensembl transcript: ENST00000404802
  gene symbol: MPST
  hgvsc: ENST00000404802.3:c.793G>A
  hgvsp: ENSP00000383950.3:p.Gly265Ser
  variant of: http://identifiers.org/hgnc/7223
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly285Ser
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 20320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.151012891344383e-4
allele num: 8688
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13698
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

DP
type: SiteQuality
SIO_000300: 1.0033e6

FS
type: SiteQuality
SIO_000300: 3.106e0

MQRankSum
type: SiteQuality
SIO_000300: -1.176e0

GenotypeQuality
all individuals: 24288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.184450581638631e-5
allele num: 47796
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.003552e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.081e0

QD
type: SiteQuality
SIO_000300: 8.1e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.131014789242637e-5
allele num: 46926
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.097e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.262029578485275e-5
allele num: 46926
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.85639e5

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.097e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.172213050656008e-5
allele num: 46036
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.579279848389134e-4
allele num: 6332
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.29e-1

DP
type: SiteQuality
SIO_000300: 9.60295e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.487e0

FS
type: SiteQuality
SIO_000300: 1.985e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

QD
type: SiteQuality
SIO_000300: 2.53e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.341031429067546e-5
allele num: 46072
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.62143891839691e-4
allele num: 8284
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 3.332275468105363e-3
allele num: 6302
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13422
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 9.57805e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-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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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.229554980825827e-5
allele num: 44852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4566
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: 1.0315e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

BaseQRankSum
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SIO_000300: -4.059e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.004e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 9.29309e5

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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

African
type: Population
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allele frequency: 1.618122977346278e-4
allele num: 6180
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.764e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.206e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 5
allele frequency: 8.573388203017832e-4
allele num: 5832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.532e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

DP
type: SiteQuality
SIO_000300: 8.8226e5

QD
type: SiteQuality
SIO_000300: 1.169e1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4208
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African
type: Population
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Other
type: Population
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Latino
type: Population
allele count: 20
allele frequency: 2.818489289740699e-3
allele num: 7096
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

DP
type: SiteQuality
SIO_000300: 8.25875e5

GenotypeQuality
all individuals: 812
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30466
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.877581674802854e-4
allele num: 5326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 6.70312e5

FS
type: SiteQuality
SIO_000300: 3.222e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

QD
type: SiteQuality
SIO_000300: 8.199999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

GenotypeQuality
all individuals: 1271
bin: 2.5e0
variant carriers: 36

GenotypeQuality
all individuals: 1271
bin: 3.25e1
variant carriers: 128

GenotypeQuality
all individuals: 775
bin: 1.25e1
variant carriers: 95

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 129

GenotypeQuality
all individuals: 202
bin: 8.25e1
variant carriers: 156

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 161

GenotypeQuality
all individuals: 1688
bin: 2.75e1
variant carriers: 73

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 186

GenotypeQuality
all individuals: 4849
bin: 9.75e1
variant carriers: 4841

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 127

GenotypeQuality
all individuals: 695
bin: 3.75e1
variant carriers: 128

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 145

Other
type: Population
allele count: 44
allele frequency: 1.0e-1
allele num: 440
num of homozygotes: 1

African
type: Population
allele count: 2388
allele frequency: 4.642301710730949e-1
allele num: 5144
num of homozygotes: 444

East Asian
type: Population
allele count: 276
allele frequency: 7.792207792207792e-2
allele num: 3542
num of homozygotes: 7

Latino
type: Population
allele count: 269
allele frequency: 6.560975609756098e-2
allele num: 4100
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 401
allele frequency: 1.307040417209909e-1
allele num: 3068
num of homozygotes: 16

South Asian
type: Population
allele count: 118
allele frequency: 1.084359492740305e-2
allele num: 10882
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 2741
allele frequency: 9.826485982648599e-2
allele num: 27894
num of homozygotes: 88

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.660000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.705e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 6.78799e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

FS
type: SiteQuality
SIO_000300: 1.943e0

GenotypeQuality
all individuals: 487
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16774
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 9.095043201455206e-5
allele num: 21990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.52033e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

VQSLOD
type: SiteQuality
SIO_000300: -5.047e-1

QD
type: SiteQuality
SIO_000300: 1.03e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5730
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.337888331376107e-5
allele num: 18734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2056
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.05044e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 7.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.69e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 22132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1962
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.566333808844508e-4
allele num: 2804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.821600771456124e-4
allele num: 2074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 4.94131e5

QD
type: SiteQuality
SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.14e0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1368
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.33e-2

DP
type: SiteQuality
SIO_000300: 3.70861e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.134e1

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9019
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.70861e5

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.384657989476599e-4
allele num: 7222
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.242236024844721e-4
allele num: 8050
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 3.4797e5

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.317e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 2.9496e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.914e0

QD
type: SiteQuality
SIO_000300: 5.17e0

GenotypeQuality
all individuals: 24756
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.253796095444685e-3
allele num: 922
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.019e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 2.62494e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.23e-2

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.057e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 1.161e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.82e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.813953488372093e-3
allele num: 516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5218
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.519e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
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FS
type: SiteQuality
SIO_000300: 6.55e-1

QD
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BaseQRankSum
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SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 2.55623e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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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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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.302761855132882e-4
allele num: 7676
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.45663e5

VQSLOD
type: SiteQuality
SIO_000300: -3.132e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.303e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

FS
type: SiteQuality
SIO_000300: 9.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.512e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.303441084462982e-4
allele num: 7672
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.41557e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.829999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 2.898e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.126e0

QD
type: SiteQuality
SIO_000300: 1.282e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.275109170305677e-3
allele num: 916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

DP
type: SiteQuality
SIO_000300: 2.07714e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

MQ
type: SiteQuality
SIO_000300: 6.033e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.775895263765884e-4
allele num: 5194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.039999999999999e-2

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.124e0

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.32e-2

DP
type: SiteQuality
SIO_000300: 1.9987e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.73e-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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.906941266209001e-4
allele num: 5244
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

FS
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.633587786259542e-4
allele num: 5240
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

VQSLOD
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FS
type: SiteQuality
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DP
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InbreedingCoeff
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QD
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 5.893e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
type: Population
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allele num: 204
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 1.900418091980236e-4
allele num: 5262
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European (Finnish)
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FS
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.318894351173361e-5
allele num: 43124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
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: 7158
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.397428731134712e-4
allele num: 7156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 7.49988e5

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 3.478e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13288
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 320
bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.31932461267279e-5
allele num: 43116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 7.54151e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
all individuals: 6978
bin: 3.25e1
variant carriers: 287

GenotypeQuality
all individuals: 1204
bin: 5.25e1
variant carriers: 162

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 59

GenotypeQuality
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variant carriers: 58

GenotypeQuality
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bin: 4.75e1
variant carriers: 212

GenotypeQuality
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bin: 8.25e1
variant carriers: 36

GenotypeQuality
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bin: 9.25e1
variant carriers: 90

GenotypeQuality
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variant carriers: 38

GenotypeQuality
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bin: 9.75e1
variant carriers: 13295

GenotypeQuality
all individuals: 218
bin: 7.75e1
variant carriers: 52

GenotypeQuality
all individuals: 5181
bin: 3.75e1
variant carriers: 286

European (Finnish)
type: Population
allele count: 521
allele frequency: 1.236355007119127e-1
allele num: 4214
num of homozygotes: 30

European (Non-Finnish)
type: Population
allele count: 8777
allele frequency: 1.995316904610348e-1
allele num: 43988
num of homozygotes: 782

East Asian
type: Population
allele count: 17
allele frequency: 2.86484664644422e-3
allele num: 5934
num of homozygotes: 0

Other
type: Population
allele count: 95
allele frequency: 1.60472972972973e-1
allele num: 592
num of homozygotes: 6

African
type: Population
allele count: 439
allele frequency: 6.066887783305694e-2
allele num: 7236
num of homozygotes: 14

South Asian
type: Population
allele count: 1048
allele frequency: 1.111582520152737e-1
allele num: 9428
num of homozygotes: 64

Latino
type: Population
allele count: 2198
allele frequency: 2.988036976617727e-1
allele num: 7356
num of homozygotes: 263

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 7.72885e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

QD
type: SiteQuality
SIO_000300: 2.192e1

GenotypeQuality
all individuals: 217
bin: 7.75e1
variant carriers: 52

GenotypeQuality
all individuals: 2152
bin: 1.75e1
variant carriers: 146

GenotypeQuality
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variant carriers: 287

GenotypeQuality
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GenotypeQuality
all individuals: 11183
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variant carriers: 209

GenotypeQuality
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variant carriers: 90

GenotypeQuality
all individuals: 741
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variant carriers: 110

GenotypeQuality
all individuals: 1603
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variant carriers: 57

GenotypeQuality
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variant carriers: 58

GenotypeQuality
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variant carriers: 161

GenotypeQuality
all individuals: 2200
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variant carriers: 162

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 39

East Asian
type: Population
allele count: 18
allele frequency: 3.015075376884422e-3
allele num: 5970
num of homozygotes: 0

Other
type: Population
allele count: 97
allele frequency: 1.611295681063123e-1
allele num: 602
num of homozygotes: 6

Latino
type: Population
allele count: 2231
allele frequency: 3.009171837065012e-1
allele num: 7414
num of homozygotes: 265

South Asian
type: Population
allele count: 1058
allele frequency: 1.115563053563897e-1
allele num: 9484
num of homozygotes: 64

African
type: Population
allele count: 443
allele frequency: 6.117094725214029e-2
allele num: 7242
num of homozygotes: 14

European (Non-Finnish)
type: Population
allele count: 8926
allele frequency: 2.013807418103059e-1
allele num: 44324
num of homozygotes: 797

European (Finnish)
type: Population
allele count: 525
allele frequency: 1.245256166982922e-1
allele num: 4216
num of homozygotes: 30

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

DP
type: SiteQuality
SIO_000300: 7.77467e5

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.58e-2

QD
type: SiteQuality
SIO_000300: 2.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 7211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
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variant carriers: 0

GenotypeQuality
all individuals: 13587
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variant carriers: 0

GenotypeQuality
all individuals: 1921
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variant carriers: 0

GenotypeQuality
all individuals: 3105
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 1

GenotypeQuality
all individuals: 180
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GenotypeQuality
all individuals: 230
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 3900
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variant carriers: 0

GenotypeQuality
all individuals: 5159
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GenotypeQuality
all individuals: 646
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44946
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.639344262295082e-3
allele num: 610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.19e-1

QD
type: SiteQuality
SIO_000300: 1.533e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 7.912e0

DP
type: SiteQuality
SIO_000300: 7.79462e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

GenotypeQuality
all individuals: 214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6580
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variant carriers: 0

GenotypeQuality
all individuals: 232
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 6291
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9517
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GenotypeQuality
all individuals: 3467
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GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 1469
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.652346331791143e-4
allele num: 6052
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

DP
type: SiteQuality
SIO_000300: 7.90885e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

QD
type: SiteQuality
SIO_000300: 1.42e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQ
type: SiteQuality
SIO_000300: 6.035e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 630
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GenotypeQuality
all individuals: 14327
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GenotypeQuality
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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: 249
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.12630236019562e-5
allele num: 47030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.663e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.798e1

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

QD
type: SiteQuality
SIO_000300: 5.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.691e0

DP
type: SiteQuality
SIO_000300: 8.59261e5

GenotypeQuality
all individuals: 1322
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 181
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GenotypeQuality
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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: 251
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variant carriers: 0

GenotypeQuality
all individuals: 5429
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.082899395959175e-5
allele num: 48010
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 9.08827e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.032e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQ
type: SiteQuality
SIO_000300: 5.413e1

VQSLOD
type: SiteQuality
SIO_000300: -1.356e0

GenotypeQuality
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bin: 5.25e1
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
all individuals: 74
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2210
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GenotypeQuality
all individuals: 680
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12802
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.83614263155962e-5
allele num: 54462
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.748e1

DP
type: SiteQuality
SIO_000300: 1.11186e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

VQSLOD
type: SiteQuality
SIO_000300: -2.348e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

FS
type: SiteQuality
SIO_000300: 4.343e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
all individuals: 725
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 598
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GenotypeQuality
all individuals: 1211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 183
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GenotypeQuality
all individuals: 660
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GenotypeQuality
all individuals: 44569
bin: 6.25e1
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GenotypeQuality
all individuals: 510
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variant carriers: 0

GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 2924
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0991426687184e-4
allele num: 9098
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14688
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.2591e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.338e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 675
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.75e1
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GenotypeQuality
all individuals: 2973
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5798
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.089087344805053e-4
allele num: 9182
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.666e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.27291e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.613267512018843e-5
allele num: 61986
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

DP
type: SiteQuality
SIO_000300: 1.291767e6

MQ
type: SiteQuality
SIO_000300: 5.827e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.432e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.235e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.713e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 291
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.246096189881324e-5
allele num: 16010
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.19e1

DP
type: SiteQuality
SIO_000300: 1.365495e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.103e0

FS
type: SiteQuality
SIO_000300: 7.952e0

MQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

GenotypeQuality
all individuals: 175
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 826
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 318
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GenotypeQuality
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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: 282
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GenotypeQuality
all individuals: 3633
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.072385400024579e-5
allele num: 65096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 4.055972419387548e-4
allele num: 9862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.887308922858158e-5
allele num: 11252
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.373687e6

QD
type: SiteQuality
SIO_000300: 1.231e1

FS
type: SiteQuality
SIO_000300: 2.024e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeQuality
all individuals: 607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 190
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GenotypeQuality
all individuals: 51446
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 288
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GenotypeQuality
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GenotypeQuality
all individuals: 318
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GenotypeQuality
all individuals: 265
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GenotypeQuality
all individuals: 333
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.133652283252063e-5
allele num: 65214
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.16e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

MQRankSum
type: SiteQuality
SIO_000300: -1.76e-1

FS
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.377212e6

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: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 271
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GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001201441730076e-4
allele num: 9988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053528352010748e-5
allele num: 65498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

QD
type: SiteQuality
SIO_000300: 9.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 5.09e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.382435e6

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3784
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.16370808678501e-5
allele num: 16224
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.414999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.604e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 8.779999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.384514e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65950
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
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 2.264e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.325e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

DP
type: SiteQuality
SIO_000300: 1.397995e6

GenotypeQuality
all individuals: 594
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GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 146
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GenotypeQuality
all individuals: 850
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GenotypeQuality
all individuals: 253
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GenotypeQuality
all individuals: 53193
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GenotypeQuality
all individuals: 73
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.510847887834653e-5
allele num: 66188
num of homozygotes: 0

ClippingRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 896
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66190
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 9.738994935722633e-5
allele num: 10268
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6530
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South Asian
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allele frequency: 0.0e0
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FS
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6542
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Latino
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allele frequency: 8.695652173913044e-5
allele num: 11500
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East Asian
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Other
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South Asian
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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Other
type: Population
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European (Non-Finnish)
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allele frequency: 1.207328483897256e-4
allele num: 66262
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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InbreedingCoeff
type: SiteQuality
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DP
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BaseQRankSum
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QD
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MQRankSum
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FS
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MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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allele num: 66310
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Other
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European (Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQ
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FS
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MQRankSum
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele frequency: 4.52447742285766e-5
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East Asian
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African
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Latino
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European (Finnish)
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Other
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DP
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MQ
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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allele num: 66334
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East Asian
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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QD
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ReadPosRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
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

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.416487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
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SIO_000300: -7.35e-1

FS
type: SiteQuality
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QD
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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MQRankSum
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SIO_000300: -1.561e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.018503426001389e-5
allele num: 66258
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.415105e6

VQSLOD
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MQ
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 2.53e-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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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
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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InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.84e0

DP
type: SiteQuality
SIO_000300: 1.414485e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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Latino
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
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MQ
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.714396735962697e-5
allele num: 10294
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 4.546005576433507e-5
allele num: 65992
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.079396923825157e-5
allele num: 65796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.396283e6

FS
type: SiteQuality
SIO_000300: 1.124e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65658
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.07e-2

QD
type: SiteQuality
SIO_000300: 3.223e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.394379e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.569826955885937e-5
allele num: 65648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.955312119631368e-4
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.796238244514106e-5
allele num: 10208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.394802e6

QD
type: SiteQuality
SIO_000300: 1.284e1

FS
type: SiteQuality
SIO_000300: 1.225e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeQuality
all individuals: 3665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52092
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.057355998532469e-5
allele num: 65416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.391748e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.045e0

FS
type: SiteQuality
SIO_000300: 6.552e0

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

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

GenotypeQuality
all individuals: 782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51841
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531393568147014e-5
allele num: 65300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.38915e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 4.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.396e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 2.729e1

MQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.597e0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.665419758385969e-5
allele num: 65228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

DP
type: SiteQuality
SIO_000300: 1.388481e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.055e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 7.285e0