15-75183953-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75183953
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75183953
    reference: chr 15
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.345+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.306+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.345+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.345+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.285+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.285+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.454+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.195+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.285+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.330+48T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+123T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.195+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.376+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.345+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.285+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.285+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.345+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.309+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*241+33T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.255+123T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.402+33T>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-75183955-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75183955
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75183955
    reference: chr 15
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*241+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.285+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.345+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.345+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.255+125C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.345+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.306+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.345+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.285+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.345+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.309+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.376+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.285+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.195+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.330+50C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.402+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.285+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+125C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.195+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.285+35C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.454+35C>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

15-75183959-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75183959
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75183959
    reference: chr 15
allele count: 2
allele frequency: 1.652564780539397e-5
allele num: 121024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.345+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.195+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.345+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.345+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.330+54A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.402+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.345+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.376+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.285+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.285+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.285+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.345+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.195+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.306+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+129A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.285+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.285+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.309+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.454+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*241+39A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.255+129A>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

15-75183962-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75183962
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75183962
    reference: chr 15
allele count: 4
allele frequency: 3.306386285109689e-5
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.285+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.255+132G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.285+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.285+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.345+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+132G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.376+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.345+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.195+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.195+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.306+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.402+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.330+57G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.345+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.285+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.345+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.309+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.285+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*241+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.345+42G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.454+42G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

15-75184953-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184953
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184953
    reference: chr 15
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1123G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.286-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-76G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.196-49G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-49G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

15-75184973-ATCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184973
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184970
    reference: chr 15
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-23_286-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-23_196-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-23_286-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.196-23_196-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-23_377-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-50_331-48delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-23_*242-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-23_346-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-23_346-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-23_455-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-23_346-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.286-23_286-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-23_346-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1149_255+1151delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-23_286-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-23_346-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-23_307-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-23_403-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-23_310-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-23_286-21delCTC
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-23_256-21delCTC
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: ATCC
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

15-75184981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184981
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184981
    reference: chr 15
allele count: 2
allele frequency: 1.653302471687195e-5
allele num: 120970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1151C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-48C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.286-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.196-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-21C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-21C>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

15-75184986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184986
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184986
    reference: chr 15
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1156C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.286-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.196-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-43C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-16C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-16C>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

15-75184990-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184990
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184990
    reference: chr 15
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.196-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1160G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-39G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.286-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-12G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-12G>A
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-75184995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75184995
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75184995
    reference: chr 15
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.403-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.286-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.346-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.346-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*242-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.346-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.286-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.310-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.286-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.346-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.286-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.346-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1165C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.196-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.377-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-34C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.307-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.455-7C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.256-7C>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.346-7C>T
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-75185005-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185005
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185005
    reference: chr 15
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.259C>G
  hgvsp: ENSP00000457494.1:p.Leu87Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.349C>G
  hgvsp: ENSP00000318192.6:p.Leu117Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.349C>G
  hgvsp: ENSP00000455405.1:p.Leu117Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.199C>G
  hgvsp: ENSP00000454312.1:p.Leu67Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.313C>G
  hgvsp: ENSP00000455065.1:p.Leu105Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.380C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.406C>G
  hgvsp: ENSP00000454622.1:p.Leu136Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.289C>G
  hgvsp: ENSP00000455161.1:p.Leu97Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.349C>G
  hgvsp: ENSP00000454619.1:p.Leu117Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.289C>G
  hgvsp: ENSP00000455477.1:p.Leu97Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.349C>G
  hgvsp: ENSP00000457885.1:p.Leu117Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.349C>G
  hgvsp: ENSP00000318318.6:p.Leu117Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*245C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.289C>G
  hgvsp: ENSP00000455383.1:p.Leu97Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.289C>G
  hgvsp: ENSP00000455241.1:p.Leu97Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-24C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.458C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.199C>G
  hgvsp: ENSP00000440447.1:p.Leu67Val
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1175C>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu117Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

15-75185017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185017
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185017
    reference: chr 15
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.361C>T
  hgvsp: ENST00000352410.4:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.361C>T
  hgvsp: ENST00000565576.1:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.301C>T
  hgvsp: ENST00000563786.1:c.301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.271C>T
  hgvsp: ENST00000568907.1:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.211C>T
  hgvsp: ENST00000535694.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.331-12C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.211C>T
  hgvsp: ENST00000564003.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.325C>T
  hgvsp: ENST00000568828.1:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.301C>T
  hgvsp: ENST00000562606.1:c.301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.361C>T
  hgvsp: ENST00000323744.6:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1187C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.301C>T
  hgvsp: ENST00000567570.1:c.301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.361C>T
  hgvsp: ENST00000566377.1:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.418C>T
  hgvsp: ENST00000569233.1:c.418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.322C>T
  hgvsp: ENST00000567177.1:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.470C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.301C>T
  hgvsp: ENST00000564633.1:c.301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.301C>T
  hgvsp: ENST00000569931.1:c.301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.361C>T
  hgvsp: ENST00000563422.1:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu121Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-75185030-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185030
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185030
    reference: chr 15
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.314C>A
  hgvsp: ENSP00000455477.1:p.Ala105Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.314C>A
  hgvsp: ENSP00000455241.1:p.Ala105Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.224C>A
  hgvsp: ENSP00000454312.1:p.Ala75Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.374C>A
  hgvsp: ENSP00000318318.6:p.Ala125Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.335C>A
  hgvsp: ENSP00000457013.1:p.Ala112Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.314C>A
  hgvsp: ENSP00000455383.1:p.Ala105Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.431C>A
  hgvsp: ENSP00000454622.1:p.Ala144Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.374C>A
  hgvsp: ENSP00000457885.1:p.Ala125Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.224C>A
  hgvsp: ENSP00000440447.1:p.Ala75Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.374C>A
  hgvsp: ENSP00000455405.1:p.Ala125Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.374C>A
  hgvsp: ENSP00000454619.1:p.Ala125Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.332C>A
  hgvsp: ENSP00000455972.1:p.Ala111Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.405C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.338C>A
  hgvsp: ENSP00000455065.1:p.Ala113Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*270C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.374C>A
  hgvsp: ENSP00000318192.6:p.Ala125Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.314C>A
  hgvsp: ENSP00000455161.1:p.Ala105Asp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.483C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1200C>A
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala125Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

15-75185033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185033
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185033
    reference: chr 15
allele count: 7
allele frequency: 5.775672865888876e-5
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.377C>T
  hgvsp: ENSP00000454619.1:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.227C>T
  hgvsp: ENSP00000440447.1:p.Pro76Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.317C>T
  hgvsp: ENSP00000455477.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.317C>T
  hgvsp: ENSP00000455161.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.341C>T
  hgvsp: ENSP00000455065.1:p.Pro114Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.317C>T
  hgvsp: ENSP00000455383.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.317C>T
  hgvsp: ENSP00000457020.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.335C>T
  hgvsp: ENSP00000455972.1:p.Pro112Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.486C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.338C>T
  hgvsp: ENSP00000457013.1:p.Pro113Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.377C>T
  hgvsp: ENSP00000457885.1:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.287C>T
  hgvsp: ENSP00000457494.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.317C>T
  hgvsp: ENSP00000455241.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.377C>T
  hgvsp: ENSP00000318318.6:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.377C>T
  hgvsp: ENSP00000455405.1:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.377C>T
  hgvsp: ENSP00000318192.6:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1203C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.408C>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro126Leu
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: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

15-75185034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185034
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185034
    reference: chr 15
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.409G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.378G>A
  hgvsp: ENST00000565576.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.228G>A
  hgvsp: ENST00000535694.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.378G>A
  hgvsp: ENST00000566377.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.342G>A
  hgvsp: ENST00000568828.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.228G>A
  hgvsp: ENST00000564003.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.378G>A
  hgvsp: ENST00000323744.6:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.378G>A
  hgvsp: ENST00000563422.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.339G>A
  hgvsp: ENST00000567177.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.318G>A
  hgvsp: ENST00000564633.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.318G>A
  hgvsp: ENST00000569931.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.336G>A
  hgvsp: ENST00000567132.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1204G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.378G>A
  hgvsp: ENST00000352410.4:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.318G>A
  hgvsp: ENST00000567570.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*274G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.288G>A
  hgvsp: ENST00000568907.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.318G>A
  hgvsp: ENST00000563786.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.435G>A
  hgvsp: ENST00000569233.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro126Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

15-75185038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185038
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185038
    reference: chr 15
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.382C>T
  hgvsp: ENSP00000457885.1:p.His128Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.491C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.322C>T
  hgvsp: ENSP00000455383.1:p.His108Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.292C>T
  hgvsp: ENSP00000457494.1:p.His98Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.382C>T
  hgvsp: ENSP00000455405.1:p.His128Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.232C>T
  hgvsp: ENSP00000440447.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*278C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.322C>T
  hgvsp: ENSP00000457020.1:p.His108Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.232C>T
  hgvsp: ENSP00000454312.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.382C>T
  hgvsp: ENSP00000318192.6:p.His128Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.382C>T
  hgvsp: ENSP00000454619.1:p.His128Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.343C>T
  hgvsp: ENSP00000457013.1:p.His115Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.346C>T
  hgvsp: ENSP00000455065.1:p.His116Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.382C>T
  hgvsp: ENSP00000318318.6:p.His128Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1208C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.439C>T
  hgvsp: ENSP00000454622.1:p.His147Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.322C>T
  hgvsp: ENSP00000455241.1:p.His108Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.413C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.340C>T
  hgvsp: ENSP00000455972.1:p.His114Tyr
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His128Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

15-75185045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185045
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185045
    reference: chr 15
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.446C>T
  hgvsp: ENSP00000454622.1:p.Pro149Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.420C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.329C>T
  hgvsp: ENSP00000455477.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.389C>T
  hgvsp: ENSP00000318192.6:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.329C>T
  hgvsp: ENSP00000455383.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*285C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.347C>T
  hgvsp: ENSP00000455972.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1215C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.239C>T
  hgvsp: ENSP00000440447.1:p.Pro80Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.329C>T
  hgvsp: ENSP00000457020.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.389C>T
  hgvsp: ENSP00000318318.6:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.389C>T
  hgvsp: ENSP00000457885.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.329C>T
  hgvsp: ENSP00000455241.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.389C>T
  hgvsp: ENSP00000454619.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.389C>T
  hgvsp: ENSP00000455405.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.299C>T
  hgvsp: ENSP00000457494.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.498C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.350C>T
  hgvsp: ENSP00000457013.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.353C>T
  hgvsp: ENSP00000455065.1:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro130Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

15-75185046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185046
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185046
    reference: chr 15
allele count: 17
allele frequency: 1.402108110783036e-4
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.348C>T
  hgvsp: ENST00000567132.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*286C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.354C>T
  hgvsp: ENST00000568828.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1216C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.330C>T
  hgvsp: ENST00000564633.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.330C>T
  hgvsp: ENST00000569931.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.330C>T
  hgvsp: ENST00000563786.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.390C>T
  hgvsp: ENST00000566377.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.390C>T
  hgvsp: ENST00000352410.4:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.390C>T
  hgvsp: ENST00000565576.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.390C>T
  hgvsp: ENST00000323744.6:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.499C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.330C>T
  hgvsp: ENST00000562606.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.390C>T
  hgvsp: ENST00000563422.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.300C>T
  hgvsp: ENST00000568907.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.421C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.240C>T
  hgvsp: ENST00000564003.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.330C>T
  hgvsp: ENST00000567570.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.351C>T
  hgvsp: ENST00000567177.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro130Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

15-75185047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185047
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185047
    reference: chr 15
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.391G>A
  hgvsp: ENSP00000455405.1:p.Asp131Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.352G>A
  hgvsp: ENSP00000457013.1:p.Asp118Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.349G>A
  hgvsp: ENSP00000455972.1:p.Asp117Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.391G>A
  hgvsp: ENSP00000318318.6:p.Asp131Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.391G>A
  hgvsp: ENSP00000318192.6:p.Asp131Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.331G>A
  hgvsp: ENSP00000455383.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.241G>A
  hgvsp: ENSP00000454312.1:p.Asp81Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.331G>A
  hgvsp: ENSP00000455477.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.331G>A
  hgvsp: ENSP00000455241.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.355G>A
  hgvsp: ENSP00000455065.1:p.Asp119Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.391G>A
  hgvsp: ENSP00000454619.1:p.Asp131Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.500G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.301G>A
  hgvsp: ENSP00000457494.1:p.Asp101Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.241G>A
  hgvsp: ENSP00000440447.1:p.Asp81Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1217G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.331G>A
  hgvsp: ENSP00000455161.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.422G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*287G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.448G>A
  hgvsp: ENSP00000454622.1:p.Asp150Asn
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp131Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/15-75185051-CCAACCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185051
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185045
    reference: chr 15
allele count: 5
allele frequency: 4.122963256151461e-5
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.339_344delCCACAA
  hgvsp: ENSP00000455241.1:p.Asn113_His114del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.339_344delCCACAA
  hgvsp: ENSP00000455477.1:p.Asn113_His114del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.339_344delCCACAA
  hgvsp: ENSP00000455161.1:p.Asn113_His114del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.249_254delCCACAA
  hgvsp: ENSP00000454312.1:p.Asn83_His84del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.339_344delCCACAA
  hgvsp: ENSP00000455383.1:p.Asn113_His114del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.456_461delCCACAA
  hgvsp: ENSP00000454622.1:p.Asn152_His153del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.399_404delCCACAA
  hgvsp: ENSP00000318318.6:p.Asn133_His134del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.399_404delCCACAA
  hgvsp: ENSP00000455405.1:p.Asn133_His134del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.339_344delCCACAA
  hgvsp: ENSP00000457020.1:p.Asn113_His114del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.309_314delCCACAA
  hgvsp: ENSP00000457494.1:p.Asn103_His104del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.357_362delCCACAA
  hgvsp: ENSP00000455972.1:p.Asn119_His120del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.399_404delCCACAA
  hgvsp: ENSP00000318192.6:p.Asn133_His134del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*295_*300delCCACAA
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.399_404delCCACAA
  hgvsp: ENSP00000454619.1:p.Asn133_His134del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.360_365delCCACAA
  hgvsp: ENSP00000457013.1:p.Asn120_His121del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.249_254delCCACAA
  hgvsp: ENSP00000440447.1:p.Asn83_His84del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.363_368delCCACAA
  hgvsp: ENSP00000455065.1:p.Asn121_His122del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.508_513delCCACAA
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn133_His134del
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: CCAACCA
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

15-75185062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185062
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185062
    reference: chr 15
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.346C>T
  hgvsp: ENSP00000455161.1:p.Pro116Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.437C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.406C>T
  hgvsp: ENSP00000455405.1:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.346C>T
  hgvsp: ENSP00000455477.1:p.Pro116Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.346C>T
  hgvsp: ENSP00000455241.1:p.Pro116Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.406C>T
  hgvsp: ENSP00000318318.6:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.346C>T
  hgvsp: ENSP00000455383.1:p.Pro116Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.406C>T
  hgvsp: ENSP00000454619.1:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.406C>T
  hgvsp: ENSP00000318192.6:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.256C>T
  hgvsp: ENSP00000440447.1:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.370C>T
  hgvsp: ENSP00000455065.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.364C>T
  hgvsp: ENSP00000455972.1:p.Pro122Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.367C>T
  hgvsp: ENSP00000457013.1:p.Pro123Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*302C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.256C>T
  hgvsp: ENSP00000454312.1:p.Pro86Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.346C>T
  hgvsp: ENSP00000457020.1:p.Pro116Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1232C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.406C>T
  hgvsp: ENSP00000457885.1:p.Pro136Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.316C>T
  hgvsp: ENSP00000457494.1:p.Pro106Ser
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro136Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

15-75185070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185070
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185070
    reference: chr 15
allele count: 72
allele frequency: 5.934815938277914e-4
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.414G>A
  hgvsp: ENSP00000457885.1:p.Met138Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.354G>A
  hgvsp: ENSP00000455241.1:p.Met118Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.354G>A
  hgvsp: ENSP00000455477.1:p.Met118Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.414G>A
  hgvsp: ENSP00000455405.1:p.Met138Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.378G>A
  hgvsp: ENSP00000455065.1:p.Met126Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.354G>A
  hgvsp: ENSP00000457020.1:p.Met118Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.354G>A
  hgvsp: ENSP00000455383.1:p.Met118Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.372G>A
  hgvsp: ENSP00000455972.1:p.Met124Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.414G>A
  hgvsp: ENSP00000454619.1:p.Met138Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.264G>A
  hgvsp: ENSP00000440447.1:p.Met88Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1240G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.445G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.414G>A
  hgvsp: ENSP00000318318.6:p.Met138Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.264G>A
  hgvsp: ENSP00000454312.1:p.Met88Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.375G>A
  hgvsp: ENSP00000457013.1:p.Met125Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.354G>A
  hgvsp: ENSP00000455161.1:p.Met118Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.523G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.324G>A
  hgvsp: ENSP00000457494.1:p.Met108Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.414G>A
  hgvsp: ENSP00000318192.6:p.Met138Ile
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met138Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-75185073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185073
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185073
    reference: chr 15
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.267C>T
  hgvsp: ENST00000535694.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.448C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.381C>T
  hgvsp: ENST00000568828.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.357C>T
  hgvsp: ENST00000564633.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.357C>T
  hgvsp: ENST00000563786.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.417C>T
  hgvsp: ENST00000566377.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.378C>T
  hgvsp: ENST00000567177.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.357C>T
  hgvsp: ENST00000569931.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.327C>T
  hgvsp: ENST00000568907.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.526C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.474C>T
  hgvsp: ENST00000569233.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.267C>T
  hgvsp: ENST00000564003.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.417C>T
  hgvsp: ENST00000352410.4:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.375C>T
  hgvsp: ENST00000567132.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.417C>T
  hgvsp: ENST00000323744.6:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.417C>T
  hgvsp: ENST00000565576.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1243C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.357C>T
  hgvsp: ENST00000562606.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455477
  ensembl transcript: ENST00000567570
  gene symbol: MPI
  hgvsc: ENST00000567570.1:c.357C>T
  hgvsp: ENST00000567570.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala139Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-75185075-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185075
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185075
    reference: chr 15
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.476T>C
  hgvsp: ENSP00000454622.1:p.Ile159Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.269T>C
  hgvsp: ENSP00000440447.1:p.Ile90Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.329T>C
  hgvsp: ENSP00000457494.1:p.Ile110Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.383T>C
  hgvsp: ENSP00000455065.1:p.Ile128Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.419T>C
  hgvsp: ENSP00000318318.6:p.Ile140Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.359T>C
  hgvsp: ENSP00000455383.1:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1245T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.419T>C
  hgvsp: ENSP00000454619.1:p.Ile140Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.419T>C
  hgvsp: ENSP00000455405.1:p.Ile140Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*315T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.359T>C
  hgvsp: ENSP00000455241.1:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.359T>C
  hgvsp: ENSP00000455161.1:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.528T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.269T>C
  hgvsp: ENSP00000454312.1:p.Ile90Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.419T>C
  hgvsp: ENSP00000318192.6:p.Ile140Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.419T>C
  hgvsp: ENSP00000457885.1:p.Ile140Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.377T>C
  hgvsp: ENSP00000455972.1:p.Ile126Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.359T>C
  hgvsp: ENSP00000457020.1:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.380T>C
  hgvsp: ENSP00000457013.1:p.Ile127Thr
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile140Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-75185079-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185079
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185079
    reference: chr 15
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.423C>A
  hgvsp: ENST00000566377.1:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.384C>A
  hgvsp: ENST00000567177.1:c.384C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.273C>A
  hgvsp: ENST00000564003.1:c.273C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.423C>A
  hgvsp: ENST00000352410.4:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.532C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.423C>A
  hgvsp: ENST00000565576.1:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.480C>A
  hgvsp: ENST00000569233.1:c.480C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.423C>A
  hgvsp: ENST00000563422.1:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.381C>A
  hgvsp: ENST00000567132.1:c.381C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.363C>A
  hgvsp: ENST00000563786.1:c.363C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.273C>A
  hgvsp: ENST00000535694.1:c.273C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.423C>A
  hgvsp: ENST00000323744.6:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.387C>A
  hgvsp: ENST00000568828.1:c.387C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.333C>A
  hgvsp: ENST00000568907.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.363C>A
  hgvsp: ENST00000569931.1:c.363C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.363C>A
  hgvsp: ENST00000562606.1:c.363C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.363C>A
  hgvsp: ENST00000564633.1:c.363C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1249C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.454C>A
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala141Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

15-75185086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185086
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185086
    reference: chr 15
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.280C>T
  hgvsp: ENSP00000440447.1:p.Pro94Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.370C>T
  hgvsp: ENSP00000457020.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*326C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.391C>T
  hgvsp: ENSP00000457013.1:p.Pro131Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.370C>T
  hgvsp: ENSP00000455383.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.430C>T
  hgvsp: ENSP00000457885.1:p.Pro144Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.430C>T
  hgvsp: ENSP00000318318.6:p.Pro144Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.430C>T
  hgvsp: ENSP00000454619.1:p.Pro144Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.370C>T
  hgvsp: ENSP00000455241.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.388C>T
  hgvsp: ENSP00000455972.1:p.Pro130Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.280C>T
  hgvsp: ENSP00000454312.1:p.Pro94Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.539C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.430C>T
  hgvsp: ENSP00000318192.6:p.Pro144Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.394C>T
  hgvsp: ENSP00000455065.1:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.461C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.340C>T
  hgvsp: ENSP00000457494.1:p.Pro114Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.370C>T
  hgvsp: ENSP00000455161.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1256C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.430C>T
  hgvsp: ENSP00000455405.1:p.Pro144Ser
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro144Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

15-75185088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185088
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185088
    reference: chr 15
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.390C>T
  hgvsp: ENST00000567132.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.489C>T
  hgvsp: ENST00000569233.1:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.432C>T
  hgvsp: ENST00000566377.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.432C>T
  hgvsp: ENST00000352410.4:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*328C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.396C>T
  hgvsp: ENST00000568828.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.372C>T
  hgvsp: ENST00000562606.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.282C>T
  hgvsp: ENST00000535694.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.432C>T
  hgvsp: ENST00000565576.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.282C>T
  hgvsp: ENST00000564003.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.342C>T
  hgvsp: ENST00000568907.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.372C>T
  hgvsp: ENST00000563786.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.463C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.393C>T
  hgvsp: ENST00000567177.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.432C>T
  hgvsp: ENST00000323744.6:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.541C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.372C>T
  hgvsp: ENST00000564633.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.372C>T
  hgvsp: ENST00000569931.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.432C>T
  hgvsp: ENST00000563422.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro144Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

15-75185110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185110
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185110
    reference: chr 15
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.364C>T
  hgvsp: ENSP00000457494.1:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.394C>T
  hgvsp: ENSP00000455241.1:p.Arg132Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.454C>T
  hgvsp: ENSP00000318318.6:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.485C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.304C>T
  hgvsp: ENSP00000454312.1:p.Arg102Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.454C>T
  hgvsp: ENSP00000454619.1:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.394C>T
  hgvsp: ENSP00000455383.1:p.Arg132Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.304C>T
  hgvsp: ENSP00000440447.1:p.Arg102Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.418C>T
  hgvsp: ENSP00000455065.1:p.Arg140Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1280C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.412C>T
  hgvsp: ENSP00000455972.1:p.Arg138Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.454C>T
  hgvsp: ENSP00000318192.6:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.454C>T
  hgvsp: ENSP00000455405.1:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.563C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.454C>T
  hgvsp: ENSP00000457885.1:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.511C>T
  hgvsp: ENSP00000454622.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.394C>T
  hgvsp: ENSP00000457020.1:p.Arg132Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.415C>T
  hgvsp: ENSP00000457013.1:p.Arg139Trp
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.394C>T
  hgvsp: ENSP00000455161.1:p.Arg132Trp
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg152Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

15-75185111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185111
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185111
    reference: chr 15
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.413G>A
  hgvsp: ENSP00000455972.1:p.Arg138Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.395G>A
  hgvsp: ENSP00000455241.1:p.Arg132Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.455G>A
  hgvsp: ENSP00000455405.1:p.Arg152Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.455G>A
  hgvsp: ENSP00000318318.6:p.Arg152Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.305G>A
  hgvsp: ENSP00000440447.1:p.Arg102Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.486G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.419G>A
  hgvsp: ENSP00000455065.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.455G>A
  hgvsp: ENSP00000318192.6:p.Arg152Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.395G>A
  hgvsp: ENSP00000455383.1:p.Arg132Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.416G>A
  hgvsp: ENSP00000457013.1:p.Arg139Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1281G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.455G>A
  hgvsp: ENSP00000457885.1:p.Arg152Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.305G>A
  hgvsp: ENSP00000454312.1:p.Arg102Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.395G>A
  hgvsp: ENSP00000457020.1:p.Arg132Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.455G>A
  hgvsp: ENSP00000454619.1:p.Arg152Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*351G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.512G>A
  hgvsp: ENSP00000454622.1:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.395G>A
  hgvsp: ENSP00000455161.1:p.Arg132Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.365G>A
  hgvsp: ENSP00000457494.1:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg152Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

15-75185111-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185111
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185111
    reference: chr 15
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.395G>T
  hgvsp: ENSP00000455161.1:p.Arg132Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.395G>T
  hgvsp: ENSP00000455241.1:p.Arg132Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.305G>T
  hgvsp: ENSP00000440447.1:p.Arg102Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.455G>T
  hgvsp: ENSP00000454619.1:p.Arg152Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.419G>T
  hgvsp: ENSP00000455065.1:p.Arg140Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.305G>T
  hgvsp: ENSP00000454312.1:p.Arg102Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.365G>T
  hgvsp: ENSP00000457494.1:p.Arg122Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.455G>T
  hgvsp: ENSP00000318192.6:p.Arg152Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.416G>T
  hgvsp: ENSP00000457013.1:p.Arg139Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.455G>T
  hgvsp: ENSP00000318318.6:p.Arg152Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.455G>T
  hgvsp: ENSP00000455405.1:p.Arg152Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.564G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.395G>T
  hgvsp: ENSP00000455383.1:p.Arg132Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.413G>T
  hgvsp: ENSP00000455972.1:p.Arg138Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.512G>T
  hgvsp: ENSP00000454622.1:p.Arg171Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1281G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.486G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.455G>T
  hgvsp: ENSP00000457885.1:p.Arg152Leu
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.395G>T
  hgvsp: ENSP00000457020.1:p.Arg132Leu
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg152Leu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

15-75185119-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185119
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185119
    reference: chr 15
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.373G>C
  hgvsp: ENSP00000457494.1:p.Glu125Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.313G>C
  hgvsp: ENSP00000454312.1:p.Glu105Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454622
  ensembl transcript: ENST00000569233
  gene symbol: MPI
  hgvsc: ENST00000569233.1:c.520G>C
  hgvsp: ENSP00000454622.1:p.Glu174Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.424G>C
  hgvsp: ENSP00000457013.1:p.Glu142Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.572G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.313G>C
  hgvsp: ENSP00000440447.1:p.Glu105Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.427G>C
  hgvsp: ENSP00000455065.1:p.Glu143Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1289G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.494G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.463G>C
  hgvsp: ENSP00000318318.6:p.Glu155Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.403G>C
  hgvsp: ENSP00000455161.1:p.Glu135Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.463G>C
  hgvsp: ENSP00000454619.1:p.Glu155Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.403G>C
  hgvsp: ENSP00000455383.1:p.Glu135Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.421G>C
  hgvsp: ENSP00000455972.1:p.Glu141Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.463G>C
  hgvsp: ENSP00000318192.6:p.Glu155Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.403G>C
  hgvsp: ENSP00000455241.1:p.Glu135Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.403G>C
  hgvsp: ENSP00000457020.1:p.Glu135Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.463G>C
  hgvsp: ENSP00000457885.1:p.Glu155Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*359G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu155Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-75185135-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185135
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185135
    reference: chr 15
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.329T>G
  hgvsp: ENSP00000454312.1:p.Phe110Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.419T>G
  hgvsp: ENSP00000455161.1:p.Phe140Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.479T>G
  hgvsp: ENSP00000318318.6:p.Phe160Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.389T>G
  hgvsp: ENSP00000457494.1:p.Phe130Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.510T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.479T>G
  hgvsp: ENSP00000457885.1:p.Phe160Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.437T>G
  hgvsp: ENSP00000455972.1:p.Phe146Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.329T>G
  hgvsp: ENSP00000440447.1:p.Phe110Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.419T>G
  hgvsp: ENSP00000455383.1:p.Phe140Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*375T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.479T>G
  hgvsp: ENSP00000454619.1:p.Phe160Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.419T>G
  hgvsp: ENSP00000455241.1:p.Phe140Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.440T>G
  hgvsp: ENSP00000457013.1:p.Phe147Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.479T>G
  hgvsp: ENSP00000455405.1:p.Phe160Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.443T>G
  hgvsp: ENSP00000455065.1:p.Phe148Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1305T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.479T>G
  hgvsp: ENSP00000318192.6:p.Phe160Cys
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.588T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.419T>G
  hgvsp: ENSP00000457020.1:p.Phe140Cys
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe160Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

15-75185139-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185139
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185139
    reference: chr 15
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.423A>G
  hgvsp: ENST00000564633.1:c.423A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.483A>G
  hgvsp: ENST00000565576.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.483A>G
  hgvsp: ENST00000563422.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.441A>G
  hgvsp: ENST00000567132.1:c.441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.483A>G
  hgvsp: ENST00000352410.4:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1309A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.423A>G
  hgvsp: ENST00000569931.1:c.423A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.483A>G
  hgvsp: ENST00000323744.6:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*379A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.423A>G
  hgvsp: ENST00000562606.1:c.423A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.483A>G
  hgvsp: ENST00000566377.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.333A>G
  hgvsp: ENST00000535694.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.592A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.333A>G
  hgvsp: ENST00000564003.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.447A>G
  hgvsp: ENST00000568828.1:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.444A>G
  hgvsp: ENST00000567177.1:c.444A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.393A>G
  hgvsp: ENST00000568907.1:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.514A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.423A>G
  hgvsp: ENST00000563786.1:c.423A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu161Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

15-75185141-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185141
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185141
    reference: chr 15
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.516A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.485A>G
  hgvsp: ENSP00000318192.6:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.485A>G
  hgvsp: ENSP00000318318.6:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.485A>G
  hgvsp: ENSP00000454619.1:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.446A>G
  hgvsp: ENSP00000457013.1:p.Lys149Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.425A>G
  hgvsp: ENSP00000455161.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.395A>G
  hgvsp: ENSP00000457494.1:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.425A>G
  hgvsp: ENSP00000455383.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1311A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.485A>G
  hgvsp: ENSP00000457885.1:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.425A>G
  hgvsp: ENSP00000457020.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.425A>G
  hgvsp: ENSP00000455241.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.443A>G
  hgvsp: ENSP00000455972.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.335A>G
  hgvsp: ENSP00000454312.1:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.449A>G
  hgvsp: ENSP00000455065.1:p.Lys150Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.485A>G
  hgvsp: ENSP00000455405.1:p.Lys162Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.335A>G
  hgvsp: ENSP00000440447.1:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.594A>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys162Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

15-75185149-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185149
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185149
    reference: chr 15
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.602T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1319T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+6T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.524T>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.487+6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-75185171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185171
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185171
    reference: chr 15
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1341G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.546G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.624G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+28G>A
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8625
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75185173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185173
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185173
    reference: chr 15
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1343G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.626G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.548G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+30G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+30G>A
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

15-75185179-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185179
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185179
    reference: chr 15
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.632G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.554G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+36G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1349G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+36G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

15-75185180-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185180
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185180
    reference: chr 15
allele count: 3
allele frequency: 2.47255464345762e-5
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.555G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.633G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1350G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+37G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+37G>T
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

15-75185182-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185182
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185182
    reference: chr 15
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1352C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.635C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.557C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+39C>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+39C>G
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

15-75185189-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185189
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185189
    reference: chr 15
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.564A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.642A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1359A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+46A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+46A>G
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

15-75185195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185195
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185195
    reference: chr 15
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.451+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.337+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.487+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.487+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.445+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.487+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.397+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.427+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.487+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000567116
  gene symbol: MPI
  hgvsc: ENST00000567116.1:n.570G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.427+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.648G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.427+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*383+52G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1365G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.427+52G>A
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

15-75185428-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185428
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185428
    reference: chr 15
allele count: 3
allele frequency: 2.476759737793703e-5
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178802
  ensembl transcript: ENST00000568840
  gene symbol: MPI
  hgvsc: ENST00000568840.1:n.881G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+285G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+285G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1598G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+285G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-51G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-51G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

15-75185443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185443
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185443
    reference: chr 15
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+300T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+300T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-36T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+300T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1613T>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

15-75185452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185452
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185452
    reference: chr 15
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+309T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+309T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1622T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-27T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+309T>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-27T>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

15-75185452-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185452
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185452
    reference: chr 15
allele count: 8
allele frequency: 6.596958801992281e-5
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+309T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+309T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+309T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1622T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-27T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-27T>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75185465-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185465
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185465
    reference: chr 15
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+322T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1635T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+322T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-14T>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+322T>G
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75185478-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185478
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185478
    reference: chr 15
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.428-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.488-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+335G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.488-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.446-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.488-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.452-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.428-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*384-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+335G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.428-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.398-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+335G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.338-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.488-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.428-1G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1648G>C
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.488-1G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-75185508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185508
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185508
    reference: chr 15
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.457G>A
  hgvsp: ENSP00000457020.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.481G>A
  hgvsp: ENSP00000455065.1:p.Asp161Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.475G>A
  hgvsp: ENSP00000455972.1:p.Asp159Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.517G>A
  hgvsp: ENSP00000455405.1:p.Asp173Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.367G>A
  hgvsp: ENSP00000440447.1:p.Asp123Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.457G>A
  hgvsp: ENSP00000455241.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.457G>A
  hgvsp: ENSP00000455383.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+365G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*413G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.427G>A
  hgvsp: ENSP00000457494.1:p.Asp143Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+365G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+365G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.517G>A
  hgvsp: ENSP00000457885.1:p.Asp173Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.517G>A
  hgvsp: ENSP00000454619.1:p.Asp173Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.517G>A
  hgvsp: ENSP00000318318.6:p.Asp173Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1678G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.457G>A
  hgvsp: ENSP00000455161.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp173Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

15-75185525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185525
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185525
    reference: chr 15
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.474C>T
  hgvsp: ENST00000564633.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.444C>T
  hgvsp: ENST00000568907.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*430C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.534C>T
  hgvsp: ENST00000566377.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.534C>T
  hgvsp: ENST00000565576.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.534C>T
  hgvsp: ENST00000563422.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.492C>T
  hgvsp: ENST00000567132.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+382C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.474C>T
  hgvsp: ENST00000569931.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.474C>T
  hgvsp: ENST00000562606.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.498C>T
  hgvsp: ENST00000568828.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.534C>T
  hgvsp: ENST00000352410.4:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.474C>T
  hgvsp: ENST00000563786.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+382C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1695C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.384C>T
  hgvsp: ENST00000535694.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+382C>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His178His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-75185547-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185547
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185547
    reference: chr 15
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.556G>T
  hgvsp: ENSP00000318318.6:p.Asp186Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.466G>T
  hgvsp: ENSP00000457494.1:p.Asp156Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.406G>T
  hgvsp: ENSP00000440447.1:p.Asp136Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+404G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.556G>T
  hgvsp: ENSP00000454619.1:p.Asp186Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.514G>T
  hgvsp: ENSP00000455972.1:p.Asp172Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.496G>T
  hgvsp: ENSP00000455383.1:p.Asp166Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.496G>T
  hgvsp: ENSP00000457020.1:p.Asp166Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*452G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.520G>T
  hgvsp: ENSP00000455065.1:p.Asp174Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.556G>T
  hgvsp: ENSP00000455405.1:p.Asp186Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+404G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.496G>T
  hgvsp: ENSP00000455241.1:p.Asp166Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.496G>T
  hgvsp: ENSP00000455161.1:p.Asp166Tyr
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+404G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1717G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.556G>T
  hgvsp: ENSP00000457885.1:p.Asp186Tyr
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp186Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

15-75185554-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185554
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185554
    reference: chr 15
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.503A>G
  hgvsp: ENSP00000455383.1:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455972
  ensembl transcript: ENST00000567132
  gene symbol: MPI
  hgvsc: ENST00000567132.1:c.521A>G
  hgvsp: ENSP00000455972.1:p.Gln174Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.527A>G
  hgvsp: ENSP00000455065.1:p.Gln176Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.563A>G
  hgvsp: ENSP00000454619.1:p.Gln188Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.563A>G
  hgvsp: ENSP00000455405.1:p.Gln188Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.413A>G
  hgvsp: ENSP00000440447.1:p.Gln138Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.563A>G
  hgvsp: ENSP00000318318.6:p.Gln188Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.563A>G
  hgvsp: ENSP00000457885.1:p.Gln188Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+411A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1724A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*459A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.503A>G
  hgvsp: ENSP00000457020.1:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.503A>G
  hgvsp: ENSP00000455161.1:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+411A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.503A>G
  hgvsp: ENSP00000455241.1:p.Gln168Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+411A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.473A>G
  hgvsp: ENSP00000457494.1:p.Gln158Arg
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln188Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

15-75185564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185564
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185564
    reference: chr 15
allele count: 39
allele frequency: 3.212891107705996e-4
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.573C>T
  hgvsp: ENST00000563422.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+421C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.423C>T
  hgvsp: ENST00000535694.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+421C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1734C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.537C>T
  hgvsp: ENST00000568828.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*469C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.573C>T
  hgvsp: ENST00000565576.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+421C>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455383
  ensembl transcript: ENST00000564633
  gene symbol: MPI
  hgvsc: ENST00000564633.1:c.513C>T
  hgvsp: ENST00000564633.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.513C>T
  hgvsp: ENST00000563786.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.513C>T
  hgvsp: ENST00000569931.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.573C>T
  hgvsp: ENST00000566377.1:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.573C>T
  hgvsp: ENST00000352410.4:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.513C>T
  hgvsp: ENST00000562606.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.483C>T
  hgvsp: ENST00000568907.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala191Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

15-75185578-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185578
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185578
    reference: chr 15
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.587G>A
  hgvsp: ENSP00000454619.1:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.527G>A
  hgvsp: ENSP00000455241.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.527G>A
  hgvsp: ENSP00000455161.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.437G>A
  hgvsp: ENSP00000440447.1:p.Ser146Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.587G>A
  hgvsp: ENSP00000455405.1:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455065
  ensembl transcript: ENST00000568828
  gene symbol: MPI
  hgvsc: ENST00000568828.1:c.551G>A
  hgvsp: ENSP00000455065.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.587G>A
  hgvsp: ENSP00000457885.1:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457494
  ensembl transcript: ENST00000568907
  gene symbol: MPI
  hgvsc: ENST00000568907.1:c.497G>A
  hgvsp: ENSP00000457494.1:p.Ser166Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.587G>A
  hgvsp: ENSP00000318318.6:p.Ser196Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1748G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+435G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+435G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*483G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+435G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.527G>A
  hgvsp: ENSP00000457020.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser196Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

15-75185590-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185590
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185590
    reference: chr 15
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+447A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.539A>G
  hgvsp: ENSP00000457020.1:p.His180Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.599A>G
  hgvsp: ENSP00000457885.1:p.His200Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.599A>G
  hgvsp: ENSP00000454619.1:p.His200Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*495A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+447A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+447A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.599A>G
  hgvsp: ENSP00000455405.1:p.His200Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1760A>G
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.449A>G
  hgvsp: ENSP00000440447.1:p.His150Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.539A>G
  hgvsp: ENSP00000455161.1:p.His180Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.599A>G
  hgvsp: ENSP00000318318.6:p.His200Arg
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.539A>G
  hgvsp: ENSP00000455241.1:p.His180Arg
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His200Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-75185591-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185591
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185591
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1761C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+448C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.600C>A
  hgvsp: ENSP00000457885.1:p.His200Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.540C>A
  hgvsp: ENSP00000455161.1:p.His180Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.540C>A
  hgvsp: ENSP00000457020.1:p.His180Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+448C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.540C>A
  hgvsp: ENSP00000455241.1:p.His180Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.600C>A
  hgvsp: ENSP00000318318.6:p.His200Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.600C>A
  hgvsp: ENSP00000454619.1:p.His200Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.600C>A
  hgvsp: ENSP00000455405.1:p.His200Gln
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+448C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*496C>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.450C>A
  hgvsp: ENSP00000440447.1:p.His150Gln
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His200Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

15-75185594-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185594
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185594
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+451G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*499G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+451G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.543G>C
  hgvsp: ENST00000563786.1:c.543G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.603G>C
  hgvsp: ENST00000352410.4:c.603G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.603G>C
  hgvsp: ENST00000563422.1:c.603G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.453G>C
  hgvsp: ENST00000535694.1:c.453G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.603G>C
  hgvsp: ENST00000566377.1:c.603G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.543G>C
  hgvsp: ENST00000569931.1:c.543G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.603G>C
  hgvsp: ENST00000565576.1:c.603G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+451G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1764G>C
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.543G>C
  hgvsp: ENST00000562606.1:c.543G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu201Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

15-75185600-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185600
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185600
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.609G>T
  hgvsp: ENSP00000457885.1:p.Lys203Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.459G>T
  hgvsp: ENSP00000440447.1:p.Lys153Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.609G>T
  hgvsp: ENSP00000318318.6:p.Lys203Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+457G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+457G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1770G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.609G>T
  hgvsp: ENSP00000455405.1:p.Lys203Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.549G>T
  hgvsp: ENSP00000455161.1:p.Lys183Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.609G>T
  hgvsp: ENSP00000454619.1:p.Lys203Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.549G>T
  hgvsp: ENSP00000457020.1:p.Lys183Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.549G>T
  hgvsp: ENSP00000455241.1:p.Lys183Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+457G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*505G>T
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys203Asn
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

15-75185602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185602
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185602
    reference: chr 15
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.611G>A
  hgvsp: ENSP00000457885.1:p.Ser204Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.611G>A
  hgvsp: ENSP00000455405.1:p.Ser204Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.551G>A
  hgvsp: ENSP00000457020.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.611G>A
  hgvsp: ENSP00000318318.6:p.Ser204Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1772G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+459G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.461G>A
  hgvsp: ENSP00000440447.1:p.Ser154Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.551G>A
  hgvsp: ENSP00000455161.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.551G>A
  hgvsp: ENSP00000455241.1:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.611G>A
  hgvsp: ENSP00000454619.1:p.Ser204Asn
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*507G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+459G>A
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+459G>A
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser204Asn
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

15-75185602-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185602
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185602
    reference: chr 15
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.611G>T
  hgvsp: ENSP00000318318.6:p.Ser204Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.611G>T
  hgvsp: ENSP00000455405.1:p.Ser204Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.461G>T
  hgvsp: ENSP00000440447.1:p.Ser154Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+459G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.551G>T
  hgvsp: ENSP00000457020.1:p.Ser184Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+459G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.611G>T
  hgvsp: ENSP00000457885.1:p.Ser204Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.611G>T
  hgvsp: ENSP00000454619.1:p.Ser204Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.551G>T
  hgvsp: ENSP00000455161.1:p.Ser184Ile
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+459G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1772G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*507G>T
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.551G>T
  hgvsp: ENSP00000455241.1:p.Ser184Ile
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser204Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

15-75185604-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185604
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185601
    reference: chr 15
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.619_621delAAG
  hgvsp: ENSP00000318318.6:p.Lys207del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454312
  ensembl transcript: ENST00000564003
  gene symbol: MPI
  hgvsc: ENST00000564003.1:c.337+467_337+469delAAG
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318192
  ensembl transcript: ENST00000323744
  gene symbol: MPI
  hgvsc: ENST00000323744.6:c.487+467_487+469delAAG
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.619_621delAAG
  hgvsp: ENSP00000454619.1:p.Lys207del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457619
  ensembl transcript: ENST00000562800
  gene symbol: MPI
  hgvsc: ENST00000562800.1:c.255+1780_255+1782delAAG
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.469_471delAAG
  hgvsp: ENSP00000440447.1:p.Lys157del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454267
  ensembl transcript: ENST00000561470
  gene symbol: MPI
  hgvsc: ENST00000561470.1:c.*515_*517delAAG
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.619_621delAAG
  hgvsp: ENSP00000455405.1:p.Lys207del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.559_561delAAG
  hgvsp: ENSP00000457020.1:p.Lys187del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.559_561delAAG
  hgvsp: ENSP00000455161.1:p.Lys187del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457885
  ensembl transcript: ENST00000563422
  gene symbol: MPI
  hgvsc: ENST00000563422.1:c.619_621delAAG
  hgvsp: ENSP00000457885.1:p.Lys207del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455241
  ensembl transcript: ENST00000563786
  gene symbol: MPI
  hgvsc: ENST00000563786.1:c.559_561delAAG
  hgvsp: ENSP00000455241.1:p.Lys187del
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457013
  ensembl transcript: ENST00000567177
  gene symbol: MPI
  hgvsc: ENST00000567177.1:c.448+467_448+469delAAG
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys207del
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: GAGA
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75185609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75185609
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75185609
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000318318
  ensembl transcript: ENST00000352410
  gene symbol: MPI
  hgvsc: ENST00000352410.4:c.618G>A
  hgvsp: ENST00000352410.4:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000457020
  ensembl transcript: ENST00000562606
  gene symbol: MPI
  hgvsc: ENST00000562606.1:c.558G>A
  hgvsp: ENST00000562606.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000440447
  ensembl transcript: ENST00000535694
  gene symbol: MPI
  hgvsc: ENST00000535694.1:c.468G>A
  hgvsp: ENST00000535694.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455405
  ensembl transcript: ENST00000566377
  gene symbol: MPI
  hgvsc: ENST00000566377.1:c.618G>A
  hgvsp: ENST00000566377.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000454619
  ensembl transcript: ENST00000565576
  gene symbol: MPI
  hgvsc: ENST00000565576.1:c.618G>A
  hgvsp: ENST00000565576.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178802
  ensembl protein: ENSP00000455161
  ensembl transcript: ENST00000569931
  gene symbol: MPI
  hgvsc: ENST00000569931.1:c.558G>A
  hgvsp: ENST00000569931.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7216
canonical: true
consequence: synonymous
filter: PASS
hgvs: p.Lys206Lys
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 6579
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 550
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4018
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4931
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8065
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 405
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2245
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8713
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7968
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6705
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1447
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35059
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

FS
type: SiteQuality
SIO_000300: 3.813e0

VQSLOD
type: SiteQuality
SIO_000300: -1.835e0

DP
type: SiteQuality
SIO_000300: 2.922482e6

MQ
type: SiteQuality
SIO_000300: 5.916e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e0

GenotypeDepth
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6705
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8063
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3986
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8709
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7958
bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6552
bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2245
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1448
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1762
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5445
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.582e0

VQSLOD
type: SiteQuality
SIO_000300: -1.167e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.921282e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 2.847e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.319e0

GenotypeDepth
all individuals: 741
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1447
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2244
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3837
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8061
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 938
bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4933
bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1032
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3340
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8693
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1762
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6704
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variant carriers: 0

GenotypeDepth
all individuals: 7933
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6469
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variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3498
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variant carriers: 0

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

GenotypeQuality
all individuals: 294
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4202
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006614552014432e-5
allele num: 66520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

QD
type: SiteQuality
SIO_000300: 1.396e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.917343e6

GenotypeDepth
all individuals: 6706
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1447
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1032
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variant carriers: 0

GenotypeDepth
all individuals: 6367
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 564
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variant carriers: 0

GenotypeDepth
all individuals: 1024
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variant carriers: 0

GenotypeDepth
all individuals: 909
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3712
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2244
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 187
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variant carriers: 0

GenotypeDepth
all individuals: 1762
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4934
bin: 5.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 8060
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8689
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variant carriers: 0

GenotypeDepth
all individuals: 7899
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 752
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3183
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35049
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3482
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3904
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 4
allele frequency: 3.880481179666278e-4
allele num: 10308
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

FS
type: SiteQuality
SIO_000300: 3.678e0

QD
type: SiteQuality
SIO_000300: 1.429e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 2.914027e6

GenotypeDepth
all individuals: 8398
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variant carriers: 0

GenotypeDepth
all individuals: 6580
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variant carriers: 0

GenotypeDepth
all individuals: 940
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3591
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variant carriers: 0

GenotypeDepth
all individuals: 5018
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variant carriers: 0

GenotypeDepth
all individuals: 240
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variant carriers: 0

GenotypeDepth
all individuals: 7905
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variant carriers: 0

GenotypeDepth
all individuals: 493
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variant carriers: 0

GenotypeDepth
all individuals: 12
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variant carriers: 0

GenotypeDepth
all individuals: 6638
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variant carriers: 0

GenotypeDepth
all individuals: 1967
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variant carriers: 0

GenotypeDepth
all individuals: 321
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variant carriers: 0

GenotypeDepth
all individuals: 389
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variant carriers: 0

GenotypeDepth
all individuals: 737
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2595
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variant carriers: 0

GenotypeDepth
all individuals: 1104
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variant carriers: 0

GenotypeDepth
all individuals: 193
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variant carriers: 0

GenotypeDepth
all individuals: 3982
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7906
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
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variant carriers: 0

GenotypeQuality
all individuals: 33594
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variant carriers: 1

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
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variant carriers: 0

GenotypeQuality
all individuals: 2370
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variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 8.4e0

VQSLOD
type: SiteQuality
SIO_000300: -4.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 4.873e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

DP
type: SiteQuality
SIO_000300: 2.524644e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.193e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.431e0

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6652
bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.153e0

MQ
type: SiteQuality
SIO_000300: 5.718e1

MQRankSum
type: SiteQuality
SIO_000300: -1.591e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

QD
type: SiteQuality
SIO_000300: 1.772e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 2.54017e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

GenotypeDepth
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4854
bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8476
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 630
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7951
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
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variant carriers: 0

GenotypeQuality
all individuals: 286
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
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variant carriers: 0

GenotypeQuality
all individuals: 6562
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variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.929384526336099e-4
allele num: 10366
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.36e1

FS
type: SiteQuality
SIO_000300: 2.163e0

DP
type: SiteQuality
SIO_000300: 2.54401e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.022e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.955e0

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.769e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

GenotypeDepth
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3591
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 577
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variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8500
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
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variant carriers: 0

GenotypeDepth
all individuals: 5020
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 8326
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7128
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 472
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variant carriers: 0

GenotypeDepth
all individuals: 4760
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7958
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variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
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variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 202
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variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 3674
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variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6530
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variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.546397e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

QD
type: SiteQuality
SIO_000300: 1.121e1

MQRankSum
type: SiteQuality
SIO_000300: -1.578e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.068e-1

GenotypeDepth
all individuals: 1696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2596
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8384
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5021
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8504
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
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variant carriers: 0

GenotypeDepth
all individuals: 7163
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4751
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 440
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7963
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6657
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 2527
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variant carriers: 0

GenotypeQuality
all individuals: 6670
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variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2355
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33677
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3375
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.548372e6

FS
type: SiteQuality
SIO_000300: 1.046e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.632e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -1.22e0

VQSLOD
type: SiteQuality
SIO_000300: 4.34e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000440447
ensembl transcript: ENST00000535694
gene symbol: MPI
hgvsc: ENST00000535694.1:c.196-7C>T
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000455383
ensembl transcript: ENST00000564633
gene symbol: MPI
hgvsc: ENST00000564633.1:c.286-7C>T
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 6661
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7967
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8416
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7242
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 5021
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 468
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4706
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33681
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3390
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.1058e1

QD
type: SiteQuality
SIO_000300: 1.367e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

DP
type: SiteQuality
SIO_000300: 2.550232e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457020
ensembl transcript: ENST00000562606
gene symbol: MPI
hgvsc: ENST00000562606.1:c.289C>G
hgvsp: ENSP00000457020.1:p.Leu97Val
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457013
ensembl transcript: ENST00000567177
gene symbol: MPI
hgvsc: ENST00000567177.1:c.310C>G
hgvsp: ENSP00000457013.1:p.Leu104Val
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 8522
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5023
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 144
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6663
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4683
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7970
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8505
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7370
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 327
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33687
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

FS
type: SiteQuality
SIO_000300: 1.097e0

QD
type: SiteQuality
SIO_000300: 1.327e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

DP
type: SiteQuality
SIO_000300: 2.553931e6

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*257C>T
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000567116
gene symbol: MPI
hgvsc: ENST00000567116.1:n.392C>T
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7983
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8556
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4648
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8534
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7494
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5024
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 389
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6665
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 229
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3488
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.116e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.22e-1

QD
type: SiteQuality
SIO_000300: 1.114e1

DP
type: SiteQuality
SIO_000300: 2.557085e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457494
ensembl transcript: ENST00000568907
gene symbol: MPI
hgvsc: ENST00000568907.1:c.284C>A
hgvsp: ENSP00000457494.1:p.Ala95Asp
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457020
ensembl transcript: ENST00000562606
gene symbol: MPI
hgvsc: ENST00000562606.1:c.314C>A
hgvsp: ENSP00000457020.1:p.Ala105Asp
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 7587
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8549
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5025
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3592
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4564
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8606
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7985
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6667
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33695
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.089e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.139e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.559e0

DP
type: SiteQuality
SIO_000300: 2.559248e6

FS
type: SiteQuality
SIO_000300: 7.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.26e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454622
ensembl transcript: ENST00000569233
gene symbol: MPI
hgvsc: ENST00000569233.1:c.434C>T
hgvsp: ENSP00000454622.1:p.Pro145Leu
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454312
ensembl transcript: ENST00000564003
gene symbol: MPI
hgvsc: ENST00000564003.1:c.227C>T
hgvsp: ENSP00000454312.1:p.Pro76Leu
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5027
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8551
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6666
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 227
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7610
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4550
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3594
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7986
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8620
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33698
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2617
bin: 7.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.553734061930783e-4
allele num: 6588
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504910352283989e-5
allele num: 66594
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

DP
type: SiteQuality
SIO_000300: 2.55982e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457020
ensembl transcript: ENST00000562606
gene symbol: MPI
hgvsc: ENST00000562606.1:c.318G>A
hgvsp: ENST00000562606.1:c.318G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000568840
gene symbol: MPI
hgvsc: ENST00000568840.1:n.487G>A
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8626
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7624
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3593
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5029
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6668
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7989
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8550
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3499
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33696
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 4.723e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.560186e6

QD
type: SiteQuality
SIO_000300: 1.052e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000455477
ensembl transcript: ENST00000567570
gene symbol: MPI
hgvsc: ENST00000567570.1:c.322C>T
hgvsp: ENSP00000455477.1:p.His108Tyr
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000455161
ensembl transcript: ENST00000569931
gene symbol: MPI
hgvsc: ENST00000569931.1:c.322C>T
hgvsp: ENSP00000455161.1:p.His108Tyr
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 7630
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8002
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6671
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4539
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5027
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8559
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8636
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3593
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33698
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3446
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2633
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 6961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 2.486e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.933e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 2.561166e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000455161
ensembl transcript: ENST00000569931
gene symbol: MPI
hgvsc: ENST00000569931.1:c.329C>T
hgvsp: ENSP00000455161.1:p.Pro110Leu
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454312
ensembl transcript: ENST00000564003
gene symbol: MPI
hgvsc: ENST00000564003.1:c.239C>T
hgvsp: ENSP00000454312.1:p.Pro80Leu
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8670
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3593
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4500
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1104
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8580
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5027
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6677
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8001
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7682
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33706
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.562808e6

VQSLOD
type: SiteQuality
SIO_000300: -1.962e0

FS
type: SiteQuality
SIO_000300: 5.631e0

QD
type: SiteQuality
SIO_000300: 3.101e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000440447
ensembl transcript: ENST00000535694
gene symbol: MPI
hgvsc: ENST00000535694.1:c.240C>T
hgvsp: ENST00000535694.1:c.240C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454622
ensembl transcript: ENST00000569233
gene symbol: MPI
hgvsc: ENST00000569233.1:c.447C>T
hgvsp: ENST00000569233.1:c.447C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 4497
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8578
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7675
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5026
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8013
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8684
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6678
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3595
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1699
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6960
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33719
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 2644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.004022695205788e-5
allele num: 66622
num of homozygotes: 0

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

South Asian
type: Population
allele count: 12
allele frequency: 7.267441860465116e-4
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
SIO_000300: 1.113e0

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

DP
type: SiteQuality
SIO_000300: 2.564011e6

QD
type: SiteQuality
SIO_000300: 1.5e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457020
ensembl transcript: ENST00000562606
gene symbol: MPI
hgvsc: ENST00000562606.1:c.331G>A
hgvsp: ENSP00000457020.1:p.Asp111Asn
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457885
ensembl transcript: ENST00000563422
gene symbol: MPI
hgvsc: ENST00000563422.1:c.391G>A
hgvsp: ENSP00000457885.1:p.Asp131Asn
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6676
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8690
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5028
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4476
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3593
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 386
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7700
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8015
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8581
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33724
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 2.563725e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.149e1

Annotation
canonical: false
consequence: inframe_deletion
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457885
ensembl transcript: ENST00000563422
gene symbol: MPI
hgvsc: ENST00000563422.1:c.399_404delCCACAA
hgvsp: ENSP00000457885.1:p.Asn133_His134del
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000567116
gene symbol: MPI
hgvsc: ENST00000567116.1:n.430_435delCCACAA
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 6679
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8592
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8013
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4479
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8690
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5028
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3593
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7735
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 739
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3520
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33728
bin: 9.75e1
variant carriers: 5

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.564773e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.94e0

FS
type: SiteQuality
SIO_000300: 2.475e0

QD
type: SiteQuality
SIO_000300: 8.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.223e1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000568840
gene symbol: MPI
hgvsc: ENST00000568840.1:n.515C>T
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454622
ensembl transcript: ENST00000569233
gene symbol: MPI
hgvsc: ENST00000569233.1:c.463C>T
hgvsp: ENSP00000454622.1:p.Pro155Ser
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5027
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2594
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 738
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4490
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8593
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8022
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6681
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7781
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1700
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8729
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3594
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33739
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.153e1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.969e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 2.528e0

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

DP
type: SiteQuality
SIO_000300: 2.566282e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*310G>A
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454622
ensembl transcript: ENST00000569233
gene symbol: MPI
hgvsc: ENST00000569233.1:c.471G>A
hgvsp: ENSP00000454622.1:p.Met157Ile
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 69
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8592
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.25e1
variant carriers: 8

GenotypeDepth
all individuals: 192
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 8730
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 7792
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3601
bin: 5.75e1
variant carriers: 10

GenotypeDepth
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 6.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4502
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2601
bin: 6.25e1
variant carriers: 7

GenotypeDepth
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1109
bin: 7.25e1
variant carriers: 4

GenotypeDepth
all individuals: 8023
bin: 4.25e1
variant carriers: 5

GenotypeDepth
all individuals: 396
bin: 9.75e1
variant carriers: 9

GenotypeDepth
all individuals: 6678
bin: 4.75e1
variant carriers: 5

GenotypeDepth
all individuals: 745
bin: 7.75e1
variant carriers: 6

GenotypeDepth
all individuals: 326
bin: 8.75e1
variant carriers: 5

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

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

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7118
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33780
bin: 9.75e1
variant carriers: 72

GenotypeQuality
all individuals: 3540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 66
allele frequency: 6.346153846153846e-3
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.499625018749062e-5
allele num: 66670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.125e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 2.569467e6

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.348e0

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*313C>T
variant of: http://identifiers.org/hgnc/7216

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457885
ensembl transcript: ENST00000563422
gene symbol: MPI
hgvsc: ENST00000563422.1:c.417C>T
hgvsp: ENST00000563422.1:c.417C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 8601
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7803
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4490
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8028
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8742
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6685
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2600
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2397
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7119
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.072e-1

QD
type: SiteQuality
SIO_000300: 1.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.568661e6

FS
type: SiteQuality
SIO_000300: 5.227e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.023e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.798e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000567116
gene symbol: MPI
hgvsc: ENST00000567116.1:n.450T>C
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7809
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5034
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6684
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4500
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8028
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8599
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8741
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3925
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33761
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3465
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2397
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.684e1

QD
type: SiteQuality
SIO_000300: 1.505e1

DP
type: SiteQuality
SIO_000300: 2.568776e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.186e0

VQSLOD
type: SiteQuality
SIO_000300: -2.751e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.12e0

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*319C>A
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 5033
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4481
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7820
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 8754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6685
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8030
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3595
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33762
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3932
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2399
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7117
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.923e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 4.225e0

QD
type: SiteQuality
SIO_000300: 1.037e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.529e0

VQSLOD
type: SiteQuality
SIO_000300: -2.676e-1

DP
type: SiteQuality
SIO_000300: 2.569206e6

MQRankSum
type: SiteQuality
SIO_000300: -5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.96e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454622
ensembl transcript: ENST00000569233
gene symbol: MPI
hgvsc: ENST00000569233.1:c.487C>T
hgvsp: ENSP00000454622.1:p.Pro163Ser
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7844
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1703
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8761
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4448
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8034
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8613
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2697
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33764
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.502e0

QD
type: SiteQuality
SIO_000300: 9.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

FS
type: SiteQuality
SIO_000300: 9.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 2.569817e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000457619
ensembl transcript: ENST00000562800
gene symbol: MPI
hgvsc: ENST00000562800.1:c.255+1258C>T
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8034
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4440
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8770
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7842
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8617
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 742
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33765
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3935
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.669e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 2.56999e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.711e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.373e1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.447e0

VQSLOD
type: SiteQuality
SIO_000300: -4.675e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*350C>T
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8040
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4397
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8807
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5034
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3597
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7842
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8630
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 742
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33770
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2409
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.571221e6

QD
type: SiteQuality
SIO_000300: 9.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.372e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.956e0

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000178802
ensembl transcript: ENST00000568840
gene symbol: MPI
hgvsc: ENST00000568840.1:n.564G>A
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 7848
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4392
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5035
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 742
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8631
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8810
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8037
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33771
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7112
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 1.176e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

VQSLOD
type: SiteQuality
SIO_000300: -4.593e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 2.571324e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*351G>T
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 5035
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8631
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7848
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8037
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4392
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 742
bin: 7.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8810
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33771
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3549
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 2.571324e6

MQ
type: SiteQuality
SIO_000300: 5.9e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.47e-1

FS
type: SiteQuality
SIO_000300: 1.176e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.593e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000455405
ensembl transcript: ENST00000566377
gene symbol: MPI
hgvsc: ENST00000566377.1:c.463G>C
hgvsp: ENSP00000455405.1:p.Glu155Gln
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8811
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8037
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4391
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6685
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3596
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7869
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1706
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8631
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3554
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33772
bin: 9.75e1
variant carriers: 2

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.138e1

DP
type: SiteQuality
SIO_000300: 2.571597e6

FS
type: SiteQuality
SIO_000300: 1.318e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

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

GenotypeDepth
all individuals: 7863
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3597
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8035
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8813
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4386
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8630
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 9.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33772
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3555
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7138
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 2.571543e6

QD
type: SiteQuality
SIO_000300: 1.582e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.663e0

VQSLOD
type: SiteQuality
SIO_000300: -9.332e-1

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8810
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7864
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8631
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5037
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4377
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8036
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3599
bin: 5.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3551
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3555
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.219e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.571491e6

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000178802
ensembl protein: ENSP00000454267
ensembl transcript: ENST00000561470
gene symbol: MPI
hgvsc: ENST00000561470.1:c.*381A>G
variant of: http://identifiers.org/hgnc/7216

GenotypeDepth
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4376
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8035
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8813
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7867
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3598
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8629
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 2.571538e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

FS
type: SiteQuality
SIO_000300: 2.024e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.95e-1

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8630
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8809
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4367
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7852
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3598
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8035
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6687
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33773
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.571223e6

FS
type: SiteQuality
SIO_000300: 6.108e0

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e0

VQSLOD
type: SiteQuality
SIO_000300: -2.195e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.638e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e0

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

GenotypeDepth
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4238
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3598
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8767
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7749
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8035
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2708
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3931
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.356e1

MQ
type: SiteQuality
SIO_000300: 5.861e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e0

FS
type: SiteQuality
SIO_000300: 4.021e0

DP
type: SiteQuality
SIO_000300: 2.568256e6

VQSLOD
type: SiteQuality
SIO_000300: -2.026e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.546e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.146e0

GenotypeDepth
all individuals: 219
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8621
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7746
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4243
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3597
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8035
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2599
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33773
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6790
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.845e0

QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.156e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.568014e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 191
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 8034
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7686
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5036
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 391
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8744
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6686
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1108
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1705
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8625
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 6.75e1
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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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South Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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num of homozygotes: 0

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

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

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

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

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

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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

South Asian
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Latino
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allele num: 11550
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Other
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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: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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allele count: 0
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QD
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ClippingRankSum
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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SIO_000300: 3.295e0

VQSLOD
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SIO_000300: 8.69e-1

InbreedingCoeff
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SIO_000300: 8.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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allele num: 66678
num of homozygotes: 0

Other
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ReadPosRankSum
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QD
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FS
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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East Asian
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Other
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Latino
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Finnish)
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South Asian
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MQRankSum
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DP
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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East Asian
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South Asian
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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Latino
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South Asian
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European (Finnish)
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MQRankSum
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DP
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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FS
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QD
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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Latino
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South Asian
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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Latino
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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European (Non-Finnish)
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DP
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African
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MQ
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VQSLOD
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FS
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QD
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DP
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MQ
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DP
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DP
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.199e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

DP
type: SiteQuality
SIO_000300: 2.310109e6

MQ
type: SiteQuality
SIO_000300: 5.861e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.249e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0