17-17070925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17070925
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17070925
    reference: chr 17
allele count: 6
allele frequency: 4.106214070626882e-4
allele num: 14612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4126G>A
  hgvsp: ENSP00000317786.6:p.Arg1376Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-4107G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-4107G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-4107G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-4107G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-4107G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2056G>A
  hgvsp: ENSP00000412147.2:p.Arg686Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13196G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4081
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg1376Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

17-17070961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17070961
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17070961
    reference: chr 17
allele count: 3
allele frequency: 2.050861361771944e-4
allele num: 14628
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-4071C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4162C>T
  hgvsp: ENSP00000317786.6:p.Thr1388Ile
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-4071C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-4071C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2092C>T
  hgvsp: ENSP00000412147.2:p.Thr698Ile
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-4071C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-4071C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13232C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr1388Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

17-17070974-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17070974
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17070974
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 14618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-4058C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-4058C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-4058C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-4058C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2105C>G
  hgvsp: ENSP00000412147.2:p.His702Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-4058C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4175C>G
  hgvsp: ENSP00000317786.6:p.His1392Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13245C>G
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 1
hgvs: p.His1392Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-17071010-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071010
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071010
    reference: chr 17
allele count: 1
allele frequency: 6.839945280437756e-5
allele num: 14620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2141C>G
  hgvsp: ENST00000414263.1:c.2141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4211C>G
  hgvsp: ENST00000313485.6:c.4211C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13281C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-4022C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-4022C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-4022C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-4022C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-4022C>G
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu1404Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

17-17071010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071010
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071010
    reference: chr 17
allele count: 1
allele frequency: 6.839945280437756e-5
allele num: 14620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2141C>T
  hgvsp: ENST00000414263.1:c.2141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-4022C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13281C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-4022C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-4022C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4211C>T
  hgvsp: ENST00000313485.6:c.4211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-4022C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-4022C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5992
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu1404Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/17-17071044-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071044
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071044
    reference: chr 17
allele count: 3
allele frequency: 2.0344500203445e-4
allele num: 14746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13315C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3988C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2175C>A
  hgvsp: ENSP00000412147.2:p.Pro726Thr
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4245C>A
  hgvsp: ENSP00000317786.6:p.Pro1416Thr
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3988C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3988C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3988C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3988C>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6306
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro1416Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-17071045-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071045
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071045
    reference: chr 17
allele count: 3
allele frequency: 2.032520325203252e-4
allele num: 14760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3987C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3987C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2176C>A
  hgvsp: ENSP00000412147.2:p.Pro726Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13316C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3987C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3987C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4246C>A
  hgvsp: ENSP00000317786.6:p.Pro1416Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3987C>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7183
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6002
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro1416Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-17071055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071055
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071055
    reference: chr 17
allele count: 1
allele frequency: 6.745817593092283e-5
allele num: 14824
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3977C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3977C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4256C>G
  hgvsp: ENST00000313485.6:c.4256C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13326C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2186C>G
  hgvsp: ENST00000414263.1:c.2186C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3977C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3977C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3977C>G
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6842
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala1419Ala
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/17-17071057-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071057
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071057
    reference: chr 17
allele count: 1
allele frequency: 6.733099919202801e-5
allele num: 14852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3975C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13328C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2188C>A
  hgvsp: ENSP00000412147.2:p.Pro730His
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3975C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3975C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3975C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3975C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4258C>A
  hgvsp: ENSP00000317786.6:p.Pro1420His
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro1420His
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-17071068-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071068
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071068
    reference: chr 17
allele count: 52
allele frequency: 3.488528109486113e-3
allele num: 14906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4269G>T
  hgvsp: ENSP00000317786.6:p.Ala1424Ser
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3964G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3964G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3964G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3964G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2199G>T
  hgvsp: ENSP00000412147.2:p.Ala734Ser
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13339G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3964G>T
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8174
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5984
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7214
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Ala1424Ser
num of homozygotes: 3
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/17-17071072-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071072
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071072
    reference: chr 17
allele count: 1
allele frequency: 6.675567423230975e-5
allele num: 14980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3960C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3960C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4273C>A
  hgvsp: ENSP00000317786.6:p.Thr1425Asn
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2203C>A
  hgvsp: ENSP00000412147.2:p.Thr735Asn
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3960C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3960C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3960C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13343C>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7698
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr1425Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

17-17071076-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071076
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071076
    reference: chr 17
allele count: 1
allele frequency: 6.657789613848202e-5
allele num: 15020
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3956G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3956G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3956G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3956G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3956G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2207G>C
  hgvsp: ENSP00000412147.2:p.Gln736His
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13347G>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4277G>C
  hgvsp: ENSP00000317786.6:p.Gln1426His
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln1426His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

17-17071097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071097
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071097
    reference: chr 17
allele count: 1
allele frequency: 6.519754857217368e-5
allele num: 15338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3935G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3935G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3935G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2228G>A
  hgvsp: ENST00000414263.1:c.2228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4298G>A
  hgvsp: ENST00000313485.6:c.4298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3935G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13368G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3935G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr1433Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

17-17071147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071147
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071147
    reference: chr 17
allele count: 1
allele frequency: 6.129704548240775e-5
allele num: 16314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3885G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3885G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3885G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3885G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2278G>A
  hgvsp: ENSP00000412147.2:p.Arg760Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4348G>A
  hgvsp: ENSP00000317786.6:p.Arg1450Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13418G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3885G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6950
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg1450Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-17071160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071160
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071160
    reference: chr 17
allele count: 19
allele frequency: 1.15839531764419e-3
allele num: 16402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2291A>G
  hgvsp: ENST00000414263.1:c.2291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3872A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3872A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3872A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4361A>G
  hgvsp: ENST00000313485.6:c.4361A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3872A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3872A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13431A>G
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7105
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly1454Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

17-17071179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071179
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071179
    reference: chr 17
allele count: 2
allele frequency: 1.221597849987784e-4
allele num: 16372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3853G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4380G>A
  hgvsp: ENSP00000317786.6:p.Asp1461Asn
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3853G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13450G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3853G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2310G>A
  hgvsp: ENSP00000412147.2:p.Asp771Asn
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3853G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3853G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp1461Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

17-17071183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071183
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071183
    reference: chr 17
allele count: 144
allele frequency: 8.806262230919765e-3
allele num: 16352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3849C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3849C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3849C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3849C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2314C>T
  hgvsp: ENSP00000412147.2:p.Ala772Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4384C>T
  hgvsp: ENSP00000317786.6:p.Ala1462Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3849C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13454C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 2.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.25e1
  variant carriers: 2
hgvs: p.Ala1462Val
num of homozygotes: 1
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

17-17071190-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071190
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071190
    reference: chr 17
allele count: 2
allele frequency: 1.229407425620851e-4
allele num: 16268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3842A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3842A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3842A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2321A>G
  hgvsp: ENST00000414263.1:c.2321A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3842A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4391A>G
  hgvsp: ENST00000313485.6:c.4391A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13461A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3842A>G
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5050
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6521
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr1464Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

17-17071195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071195
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071195
    reference: chr 17
allele count: 1
allele frequency: 6.169031462060457e-5
allele num: 16210
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3837G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3837G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13466G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3837G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3837G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3837G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4396G>A
  hgvsp: ENSP00000317786.6:p.Arg1466His
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2326G>A
  hgvsp: ENSP00000412147.2:p.Arg776His
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1466His
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/17-17071223-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071223
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071223
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 14512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13494C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3809C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3809C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3809C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3809C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3809C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2354C>A
  hgvsp: ENSP00000412147.2:p.Ser785Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4424C>A
  hgvsp: ENSP00000317786.6:p.Ser1475Arg
  variant of: http://identifiers.org/hgnc/30321
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser1475Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

17-17071253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071253
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071253
    reference: chr 17
allele count: 1
allele frequency: 8.833922261484099e-5
allele num: 11320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3779C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+24C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+24C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13524C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3779C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3779C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3779C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3779C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

17-17071261-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17071261
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17071258
    reference: chr 17
allele count: 44
allele frequency: 4.308656482569526e-3
allele num: 10212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-3768_2164-3766delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.1227_1229delAGA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-3768_1582-3766delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-3768_2164-3766delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+35_4430+37delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+35_2360+37delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-3768_2050-3766delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-3768_2164-3766delTTC
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+13535_64+13537delTTC
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 9.75e1
  variant carriers: 58
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: ATCT
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

17-17072041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072041
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072041
    reference: chr 17
allele count: 53
allele frequency: 9.608411892675852e-3
allele num: 5516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2991C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2991C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14312C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2991C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+812C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.450G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2991C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+812C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2991C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-17072067-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072067
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072067
    reference: chr 17
allele count: 1
allele frequency: 1.601024655779699e-4
allele num: 6246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+838T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2965T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.424A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14338T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+838T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2965T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2965T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2965T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2965T>C
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

17-17072069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072069
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072069
    reference: chr 17
allele count: 1
allele frequency: 1.589319771137953e-4
allele num: 6292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2963C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14340C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.422G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+840C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2963C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2963C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+840C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2963C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2963C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

17-17072071-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072071
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072071
    reference: chr 17
allele count: 2
allele frequency: 3.102699348433137e-4
allele num: 6446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+842C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+842C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2961C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2961C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2961C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14342C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.420G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2961C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2961C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

17-17072118-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072118
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072118
    reference: chr 17
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2914T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2914T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2914T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+889T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2914T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2914T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.373A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+889T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14389T>C
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

17-17072123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072123
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072123
    reference: chr 17
allele count: 1
allele frequency: 8.400537634408603e-5
allele num: 11904
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2909C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2909C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2909C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+894C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+894C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14394C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.368G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2909C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2909C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

17-17072138-TGGCAGAGCCAGGCGCGCACACAGCCAGCACCATTGTGCTGCAAGCTCCTGACTCCCAGGTGGCTGCCACTGCTCCTGCCTACACATCCTCACAGCCACTGTCTAGCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072138
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072031
    reference: chr 17
allele count: 1
allele frequency: 7.271669575334496e-5
allele num: 13752
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: TGGCAGAGCCAGGCGCGCACACAGCCAGCACCATTGTGCTGCAAGCTCCTGACTCCCAGGTGGCTGCCACTGCTCCTGCCTACACATCCTCACAGCCACTGTCTAGCA
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-17072151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072151
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072151
    reference: chr 17
allele count: 2
allele frequency: 1.412429378531073e-4
allele num: 14160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2881C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+922C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2881C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+922C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.340G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14422C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2881C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2881C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2881C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

17-17072167-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072167
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072167
    reference: chr 17
allele count: 1
allele frequency: 6.909894969596462e-5
allele num: 14472
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2865A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.324T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2865A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2865A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2865A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+938A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+938A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2865A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14438A>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS

17-17072170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072170
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072170
    reference: chr 17
allele count: 1
allele frequency: 6.923289947382996e-5
allele num: 14444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2862A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+941A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+941A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2862A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2862A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2862A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.321T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14441A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2862A>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

17-17072234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072234
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072234
    reference: chr 17
allele count: 1
allele frequency: 6.923289947382996e-5
allele num: 14444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14505C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2798C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2798C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.257G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1005C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2798C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1005C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2798C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2798C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

17-17072267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072267
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072267
    reference: chr 17
allele count: 145
allele frequency: 9.954689001784979e-3
allele num: 14566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1038C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2765C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1038C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14538C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2765C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.224G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2765C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2765C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2765C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 9.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 2
num of homozygotes: 6
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-17072268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072268
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072268
    reference: chr 17
allele count: 3
allele frequency: 2.05874279440022e-4
allele num: 14572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2764G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2764G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1039G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2764G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2764G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.223C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1039G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2764G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14539G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5050
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

17-17072327-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072327
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072327
    reference: chr 17
allele count: 1
allele frequency: 6.929046563192905e-5
allele num: 14432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1098T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14598T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1098T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2705T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2705T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2705T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.164A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2705T>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2705T>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

17-17072329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072329
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072329
    reference: chr 17
allele count: 52
allele frequency: 3.607103218645949e-3
allele num: 14416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2703G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2703G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1100G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.162C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1100G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2703G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14600G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2703G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2703G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 9.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 2
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

17-17072333-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072333
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072333
    reference: chr 17
allele count: 1
allele frequency: 6.951202558042541e-5
allele num: 14386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2699C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14604C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2699C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2699C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2699C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1104C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1104C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.158G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2699C>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

17-17072351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072351
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072351
    reference: chr 17
allele count: 7
allele frequency: 4.999285816311955e-4
allele num: 14002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1122G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.140C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2681G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2681G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2681G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2681G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1122G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2681G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14622G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

17-17072361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072361
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072361
    reference: chr 17
allele count: 19
allele frequency: 1.390515222482436e-3
allele num: 13664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1132G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2671G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2671G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1132G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14632G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2671G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.130C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2671G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2671G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-17072389-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072389
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072389
    reference: chr 17
allele count: 1
allele frequency: 8.933357155619081e-5
allele num: 11194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1160C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1160C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2643C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14660C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2643C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2643C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.102G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2643C>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2643C>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

17-17072466-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17072466
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17072466
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 3562
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-43T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-2566A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2360+1237A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-2566A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-2566A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-2566A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-2566A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.64+14737A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4430+1237A>G
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

17-17074991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17074991
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17074991
    reference: chr 17
allele count: 1
allele frequency: 8.43554400823309e-6
allele num: 118546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4431-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2361-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2568C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.632-41G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13185G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-41G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33745
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

17-17074992-TAAAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17074992
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17074988
    reference: chr 17
allele count: 1
allele frequency: 8.436397995511836e-6
allele num: 118534
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-33_2164-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-33_2164-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-33_2164-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13177_65-13174delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2573_68-2570delCTTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.632-33_632-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2361-33_2361-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4431-33_4431-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-33_1582-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-33_2050-30delAGAA
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: TAAAG
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-17075005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075005
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075005
    reference: chr 17
allele count: 2
allele frequency: 1.677064466358087e-5
allele num: 119256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2361-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2582G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13171C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.632-27C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4431-27C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/17-17075014-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075014
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075014
    reference: chr 17
allele count: 12
allele frequency: 9.980703972320181e-5
allele num: 120232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13162C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2591G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4431-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2361-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-18C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.632-18C>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19963
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11319
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

17-17075021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075021
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075021
    reference: chr 17
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2164-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2164-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.632-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4431-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1582-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13155G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2164-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2050-11G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2598C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2361-11G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20135
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-17075036-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075036
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075036
    reference: chr 17
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2365C>A
  hgvsp: ENSP00000412147.2:p.Thr789Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2613G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4435C>A
  hgvsp: ENSP00000317786.6:p.Thr1479Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13140C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1586C>A
  hgvsp: ENSP00000462688.1:p.Thr529Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.3C>A
  hgvsp: ENSP00000411723.3:p.Thr2Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2168C>A
  hgvsp: ENSP00000379149.3:p.Thr723Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2054C>A
  hgvsp: ENSP00000400189.1:p.Thr685Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2168C>A
  hgvsp: ENSP00000342379.4:p.Thr723Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2168C>A
  hgvsp: ENSP00000379156.4:p.Thr723Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.636C>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr723Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

17-17075037-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075037
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075037
    reference: chr 17
allele count: 8
allele frequency: 6.610914620037682e-5
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.4G>A
  hgvsp: ENST00000429184.3:c.4G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2169G>A
  hgvsp: ENST00000395804.3:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2614C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13139G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1587G>A
  hgvsp: ENST00000584067.1:c.1587G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2366G>A
  hgvsp: ENST00000414263.1:c.2366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.637G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2055G>A
  hgvsp: ENST00000444976.1:c.2055G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2169G>A
  hgvsp: ENST00000395811.5:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2169G>A
  hgvsp: ENST00000341712.4:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4436G>A
  hgvsp: ENST00000313485.6:c.4436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Thr723Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

17-17075040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075040
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075040
    reference: chr 17
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2058C>T
  hgvsp: ENST00000444976.1:c.2058C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2172C>T
  hgvsp: ENST00000395804.3:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2172C>T
  hgvsp: ENST00000395811.5:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4439C>T
  hgvsp: ENST00000313485.6:c.4439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2172C>T
  hgvsp: ENST00000341712.4:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2369C>T
  hgvsp: ENST00000414263.1:c.2369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.7C>T
  hgvsp: ENST00000429184.3:c.7C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.640C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1590C>T
  hgvsp: ENST00000584067.1:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2617G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13136C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys724Cys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-17075045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075045
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075045
    reference: chr 17
allele count: 2
allele frequency: 1.651336757104876e-5
allele num: 121114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2177G>A
  hgvsp: ENSP00000342379.4:p.Arg726Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.645G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4444G>A
  hgvsp: ENSP00000317786.6:p.Arg1482Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2177G>A
  hgvsp: ENSP00000379149.3:p.Arg726Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.12G>A
  hgvsp: ENSP00000411723.3:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2374G>A
  hgvsp: ENSP00000412147.2:p.Arg792Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1595G>A
  hgvsp: ENSP00000462688.1:p.Arg532Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2177G>A
  hgvsp: ENSP00000379156.4:p.Arg726Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13131G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2063G>A
  hgvsp: ENSP00000400189.1:p.Arg688Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2622C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg726Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

17-17075049-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075049
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075049
    reference: chr 17
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.649G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2626C>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2181G>T
  hgvsp: ENST00000395811.5:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2181G>T
  hgvsp: ENST00000395804.3:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13127G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2378G>T
  hgvsp: ENST00000414263.1:c.2378G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2067G>T
  hgvsp: ENST00000444976.1:c.2067G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1599G>T
  hgvsp: ENST00000584067.1:c.1599G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2181G>T
  hgvsp: ENST00000341712.4:c.2181G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.16G>T
  hgvsp: ENST00000429184.3:c.16G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4448G>T
  hgvsp: ENST00000313485.6:c.4448G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly727Gly
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

17-17075065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075065
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075065
    reference: chr 17
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.32G>A
  hgvsp: ENSP00000411723.3:p.Glu12Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.665G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2197G>A
  hgvsp: ENSP00000379156.4:p.Glu733Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2642C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1615G>A
  hgvsp: ENSP00000462688.1:p.Glu539Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2197G>A
  hgvsp: ENSP00000342379.4:p.Glu733Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2197G>A
  hgvsp: ENSP00000379149.3:p.Glu733Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4464G>A
  hgvsp: ENSP00000317786.6:p.Glu1489Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2394G>A
  hgvsp: ENSP00000412147.2:p.Glu799Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2083G>A
  hgvsp: ENSP00000400189.1:p.Glu695Lys
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13111G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu733Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

17-17075070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075070
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075070
    reference: chr 17
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2202G>A
  hgvsp: ENST00000341712.4:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2088G>A
  hgvsp: ENST00000444976.1:c.2088G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.670G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4469G>A
  hgvsp: ENST00000313485.6:c.4469G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1620G>A
  hgvsp: ENST00000584067.1:c.1620G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13106G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2202G>A
  hgvsp: ENST00000395804.3:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2647C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.37G>A
  hgvsp: ENST00000429184.3:c.37G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2202G>A
  hgvsp: ENST00000395811.5:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2399G>A
  hgvsp: ENST00000414263.1:c.2399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr734Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

17-17075074-CAGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075074
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075071
    reference: chr 17
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1631_1633delAGA
  hgvsp: ENSP00000462688.1:p.Lys544del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2654_68-2652delTCT
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2213_2215delAGA
  hgvsp: ENSP00000342379.4:p.Lys738del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4480_4482delAGA
  hgvsp: ENSP00000317786.6:p.Lys1494del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.681_683delAGA
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2213_2215delAGA
  hgvsp: ENSP00000379156.4:p.Lys738del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2213_2215delAGA
  hgvsp: ENSP00000379149.3:p.Lys738del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2410_2412delAGA
  hgvsp: ENSP00000412147.2:p.Lys804del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2099_2101delAGA
  hgvsp: ENSP00000400189.1:p.Lys700del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.48_50delAGA
  hgvsp: ENSP00000411723.3:p.Lys17del
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13095_65-13093delAGA
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys738del
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: CAGA
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

17-17075085-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075085
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075085
    reference: chr 17
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2217T>C
  hgvsp: ENST00000395811.5:c.2217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13091T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.685T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2414T>C
  hgvsp: ENST00000414263.1:c.2414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2217T>C
  hgvsp: ENST00000395804.3:c.2217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1635T>C
  hgvsp: ENST00000584067.1:c.1635T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.52T>C
  hgvsp: ENST00000429184.3:c.52T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2103T>C
  hgvsp: ENST00000444976.1:c.2103T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4484T>C
  hgvsp: ENST00000313485.6:c.4484T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2662A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2217T>C
  hgvsp: ENST00000341712.4:c.2217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile739Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

17-17075110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075110
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075110
    reference: chr 17
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4509C>T
  hgvsp: ENSP00000317786.6:p.Arg1504Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1660C>T
  hgvsp: ENSP00000462688.1:p.Arg554Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2242C>T
  hgvsp: ENSP00000379156.4:p.Arg748Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.710C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13066C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2242C>T
  hgvsp: ENSP00000342379.4:p.Arg748Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.77C>T
  hgvsp: ENSP00000411723.3:p.Arg27Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2687G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2439C>T
  hgvsp: ENSP00000412147.2:p.Arg814Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2128C>T
  hgvsp: ENSP00000400189.1:p.Arg710Trp
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2242C>T
  hgvsp: ENSP00000379149.3:p.Arg748Trp
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg748Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-17075111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075111
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075111
    reference: chr 17
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.78G>A
  hgvsp: ENSP00000411723.3:p.Arg27Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2243G>A
  hgvsp: ENSP00000379156.4:p.Arg748Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2129G>A
  hgvsp: ENSP00000400189.1:p.Arg710Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13065G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4510G>A
  hgvsp: ENSP00000317786.6:p.Arg1504Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1661G>A
  hgvsp: ENSP00000462688.1:p.Arg554Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2243G>A
  hgvsp: ENSP00000342379.4:p.Arg748Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2440G>A
  hgvsp: ENSP00000412147.2:p.Arg814Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.711G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2243G>A
  hgvsp: ENSP00000379149.3:p.Arg748Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2688C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg748Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

17-17075127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075127
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075127
    reference: chr 17
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2259T>C
  hgvsp: ENST00000341712.4:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4526T>C
  hgvsp: ENST00000313485.6:c.4526T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2145T>C
  hgvsp: ENST00000444976.1:c.2145T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2259T>C
  hgvsp: ENST00000395811.5:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2704A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.94T>C
  hgvsp: ENST00000429184.3:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1677T>C
  hgvsp: ENST00000584067.1:c.1677T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2456T>C
  hgvsp: ENST00000414263.1:c.2456T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13049T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.727T>C
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2259T>C
  hgvsp: ENST00000395804.3:c.2259T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu753Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

17-17075129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075129
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075129
    reference: chr 17
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1679G>A
  hgvsp: ENSP00000462688.1:p.Arg560Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2706C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.96G>A
  hgvsp: ENSP00000411723.3:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13047G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4528G>A
  hgvsp: ENSP00000317786.6:p.Arg1510Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2261G>A
  hgvsp: ENSP00000379149.3:p.Arg754Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.729G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2261G>A
  hgvsp: ENSP00000342379.4:p.Arg754Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2261G>A
  hgvsp: ENSP00000379156.4:p.Arg754Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2147G>A
  hgvsp: ENSP00000400189.1:p.Arg716Gln
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2458G>A
  hgvsp: ENSP00000412147.2:p.Arg820Gln
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11382
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg754Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

17-17075138-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075138
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075138
    reference: chr 17
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2467A>G
  hgvsp: ENSP00000412147.2:p.Lys823Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.105A>G
  hgvsp: ENSP00000411723.3:p.Lys36Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2270A>G
  hgvsp: ENSP00000342379.4:p.Lys757Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2270A>G
  hgvsp: ENSP00000379149.3:p.Lys757Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.738A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4537A>G
  hgvsp: ENSP00000317786.6:p.Lys1513Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1688A>G
  hgvsp: ENSP00000462688.1:p.Lys563Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2156A>G
  hgvsp: ENSP00000400189.1:p.Lys719Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2270A>G
  hgvsp: ENSP00000379156.4:p.Lys757Arg
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13038A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2715T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys757Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-17075142-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075142
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075142
    reference: chr 17
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4541C>A
  hgvsp: ENSP00000317786.6:p.Asp1514Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2160C>A
  hgvsp: ENSP00000400189.1:p.Asp720Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2471C>A
  hgvsp: ENSP00000412147.2:p.Asp824Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13034C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.109C>A
  hgvsp: ENSP00000411723.3:p.Asp37Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2274C>A
  hgvsp: ENSP00000379156.4:p.Asp758Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1692C>A
  hgvsp: ENSP00000462688.1:p.Asp564Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.742C>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2274C>A
  hgvsp: ENSP00000342379.4:p.Asp758Glu
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2719G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2274C>A
  hgvsp: ENSP00000379149.3:p.Asp758Glu
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp758Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

17-17075154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075154
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075154
    reference: chr 17
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4553C>T
  hgvsp: ENST00000313485.6:c.4553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2286C>T
  hgvsp: ENST00000395804.3:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.121C>T
  hgvsp: ENST00000429184.3:c.121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2731G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2286C>T
  hgvsp: ENST00000341712.4:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1704C>T
  hgvsp: ENST00000584067.1:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2483C>T
  hgvsp: ENST00000414263.1:c.2483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2286C>T
  hgvsp: ENST00000395811.5:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13022C>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2172C>T
  hgvsp: ENST00000444976.1:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133030
  ensembl transcript: ENST00000578548
  gene symbol: MPRIP
  hgvsc: ENST00000578548.1:n.754C>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala762Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-17075166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075166
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075166
    reference: chr 17
allele count: 3
allele frequency: 2.501125506477915e-5
allele num: 119946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1716G>A
  hgvsp: ENST00000584067.1:c.1716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.133G>A
  hgvsp: ENST00000429184.3:c.133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2298G>A
  hgvsp: ENST00000395811.5:c.2298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4565G>A
  hgvsp: ENST00000313485.6:c.4565G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2495G>A
  hgvsp: ENST00000414263.1:c.2495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13010G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2298G>A
  hgvsp: ENST00000395804.3:c.2298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2298G>A
  hgvsp: ENST00000341712.4:c.2298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2743C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2184G>A
  hgvsp: ENST00000444976.1:c.2184G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala766Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-17075173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075173
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075173
    reference: chr 17
allele count: 1
allele frequency: 8.405339071378139e-6
allele num: 118972
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2305A>G
  hgvsp: ENSP00000379156.4:p.Ile769Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2502A>G
  hgvsp: ENSP00000412147.2:p.Ile835Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2305A>G
  hgvsp: ENSP00000342379.4:p.Ile769Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4572A>G
  hgvsp: ENSP00000317786.6:p.Ile1525Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.140A>G
  hgvsp: ENSP00000411723.3:p.Ile48Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2191A>G
  hgvsp: ENSP00000400189.1:p.Ile731Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2305A>G
  hgvsp: ENSP00000379149.3:p.Ile769Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1723A>G
  hgvsp: ENSP00000462688.1:p.Ile575Val
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-13003A>G
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2750T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9752
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile769Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-17075180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075180
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075180
    reference: chr 17
allele count: 1
allele frequency: 8.411843876177658e-6
allele num: 118880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-12996G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4578+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2311+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1729+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2311+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2757C>T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2508+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2311+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2197+1G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.146+1G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5566
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2311+1G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

17-17075180-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075180
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075179
    reference: chr 17
allele count: 17830
allele frequency: 1.499831763122476e-1
allele num: 118880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4578+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2311+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-12994delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2197+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.146+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1729+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2311+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2311+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2508+3delT
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2758delA
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.25e1
  variant carriers: 1929
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.75e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.75e1
  variant carriers: 899
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 3.75e1
  variant carriers: 2190
genotype depth: GenotypeDepth
  all individuals: 19935
  bin: 2.75e1
  variant carriers: 1472
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 387
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 1185
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.25e1
  variant carriers: 726
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 2.25e1
  variant carriers: 891
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.75e1
  variant carriers: 1577
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 3.25e1
  variant carriers: 1937
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.25e1
  variant carriers: 496
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.75e1
  variant carriers: 623
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 7.25e1
  variant carriers: 73
hgvs: c.2311+3delT
num of homozygotes: 1946
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: GT
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-17075184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075184
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075184
    reference: chr 17
allele count: 4
allele frequency: 3.384782020037909e-5
allele num: 118176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4578+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2311+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.146+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2311+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-12992G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1729+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2508+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2761C>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2311+5G>A
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2197+5G>A
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12295
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2311+5G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

17-17075186-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075186
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075186
    reference: chr 17
allele count: 1
allele frequency: 8.473570932262274e-6
allele num: 118014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4578+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379156
  ensembl transcript: ENST00000395811
  gene symbol: MPRIP
  hgvsc: ENST00000395811.5:c.2311+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000379149
  ensembl transcript: ENST00000395804
  gene symbol: MPRIP
  hgvsc: ENST00000395804.3:c.2311+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2311+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2197+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000462688
  ensembl transcript: ENST00000584067
  gene symbol: MPRIP
  hgvsc: ENST00000584067.1:c.1729+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000464983
  ensembl transcript: ENST00000579832
  gene symbol: MPRIP
  hgvsc: ENST00000579832.1:c.65-12990G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000411723
  ensembl transcript: ENST00000429184
  gene symbol: MPRIP
  hgvsc: ENST00000429184.3:c.146+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2508+7G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000263624
  ensembl transcript: ENST00000584203
  gene symbol: RP11-45M22.3
  hgvsc: ENST00000584203.1:n.68-2763C>A
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25102
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3112
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2311+7G>T
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

17-17075188-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17075188
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 17075188
    reference: chr 17
allele count: 2
allele frequency: 1.698802344347235e-5
allele num: 117730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000317786
  ensembl transcript: ENST00000313485
  gene symbol: MPRIP
  hgvsc: ENST00000313485.6:c.4578+9G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000412147
  ensembl transcript: ENST00000414263
  gene symbol: MPRIP
  hgvsc: ENST00000414263.1:c.2508+9G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000400189
  ensembl transcript: ENST00000444976
  gene symbol: MPRIP
  hgvsc: ENST00000444976.1:c.2197+9G>T
  variant of: http://identifiers.org/hgnc/30321
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133030
  ensembl protein: ENSP00000342379
  ensembl transcript: ENST00000341712
  gene symbol: MPRIP
  hgvsc: ENST00000341712.4:c.2311+9G>T
  variant of: http://identifiers.org/hgnc/30321
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.040816326530612e-3
allele num: 490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5066
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 5.482456140350877e-3
allele num: 912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.075e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 1.99377e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.65e-2

FS
type: SiteQuality
SIO_000300: 1.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.282275711159737e-3
allele num: 914
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.92e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 2.01859e5

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.898e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

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

GenotypeQuality
all individuals: 4929
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6008
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.06e-2

DP
type: SiteQuality
SIO_000300: 2.02011e5

QD
type: SiteQuality
SIO_000300: 1.158e1

GenotypeQuality
all individuals: 96
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5417
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.388888888888889e-2
allele num: 72
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.04045e5

QD
type: SiteQuality
SIO_000300: 1.004e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.37e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.934e-1

FS
type: SiteQuality
SIO_000300: 1.534e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5417
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

African
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: 7666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.040816326530612e-3
allele num: 490
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.934e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.37e-2

FS
type: SiteQuality
SIO_000300: 1.534e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 2.04045e5

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5987
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5064
num of homozygotes: 0

African
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: 7662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.685393258426966e-2
allele num: 178
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.716e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.26e-2

FS
type: SiteQuality
SIO_000300: 7.033e0

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 2.08696e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

QD
type: SiteQuality
SIO_000300: 2.157e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6524
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

African
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: 5066
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 1.595744680851064e-2
allele num: 188
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.732e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 5.385e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 2.09282e5

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.1e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.34e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.485e0

VQSLOD
type: SiteQuality
SIO_000300: -2.069e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

DP
type: SiteQuality
SIO_000300: 2.11241e5

QD
type: SiteQuality
SIO_000300: 1.072e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.153e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304801670146138e-4
allele num: 7664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5092
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.65e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.424e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 1.789e1

DP
type: SiteQuality
SIO_000300: 2.11857e5

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.098901098901099e-3
allele num: 910
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 2.348030263501174e-3
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

East Asian
type: Population
allele count: 33
allele frequency: 6.790123456790123e-2
allele num: 486
num of homozygotes: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.15565e5

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.527e0

FS
type: SiteQuality
SIO_000300: 1.096e0

QD
type: SiteQuality
SIO_000300: 1.313e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

African
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: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5090
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.94e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -8.915999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.14031e5

FS
type: SiteQuality
SIO_000300: 3.043e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.308e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5084
num of homozygotes: 0

African
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: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.1463e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.543e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.98e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.834e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 3.329e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-1

QD
type: SiteQuality
SIO_000300: 9.18e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1034
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: -1.656e0

FS
type: SiteQuality
SIO_000300: 4.591e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 2.17818e5

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.319e1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.888930865130336e-4
allele num: 5294
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

FS
type: SiteQuality
SIO_000300: 9.49e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.291e1

DP
type: SiteQuality
SIO_000300: 2.25995e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 5.791505791505791e-3
allele num: 1554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.132502831257078e-3
allele num: 5298
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.217845030002609e-4
allele num: 7666
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.27275e5

QD
type: SiteQuality
SIO_000300: 1.437e1

FS
type: SiteQuality
SIO_000300: 2.528e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.45e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1588
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 2.083333333333333e-3
allele num: 480
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5268
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.309929263819754e-4
allele num: 7634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.91e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

FS
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.22594e5

QD
type: SiteQuality
SIO_000300: 1.094e1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.48e-1

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 227
bin: 7.25e1
variant carriers: 2

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

South Asian
type: Population
allele count: 4
allele frequency: 5.245213742460005e-4
allele num: 7626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 2.097902097902098e-2
allele num: 286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 56
allele frequency: 6.140350877192982e-2
allele num: 912
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 78
allele frequency: 1.484018264840183e-2
allele num: 5256
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

FS
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.22336e5

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 81
bin: 1.75e1
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GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.920122887864823e-4
allele num: 5208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.158e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 2.16804e5

FS
type: SiteQuality
SIO_000300: 8.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeQuality
all individuals: 45
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
bin: 4.75e1
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GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.321003963011889e-4
allele num: 7570
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.772e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 2.288e0

MQRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.48e-2

DP
type: SiteQuality
SIO_000300: 2.15732e5

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 4558
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.033e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.85e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.79963e5

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 877
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.229157378510923e-4
allele num: 4486
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.24975e5

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.811e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.216e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.031e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

GenotypeQuality
all individuals: 3114
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 634
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variant carriers: 0

GenotypeQuality
all individuals: 448
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1078
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GenotypeQuality
all individuals: 108
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 672
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variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 6.84931506849315e-3
allele num: 146
num of homozygotes: 0

South Asian
type: Population
allele count: 43
allele frequency: 1.149118118653127e-2
allele num: 3742
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-2

FS
type: SiteQuality
SIO_000300: 5.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 5.492e1

QD
type: SiteQuality
SIO_000300: 1.69e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

DP
type: SiteQuality
SIO_000300: 1.16108e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 3959
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 782
bin: 9.75e1
variant carriers: 52

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.470588235294118e-2
allele num: 136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.006410256410256e-4
allele num: 2496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

African
type: Population
allele count: 50
allele frequency: 7.621951219512195e-2
allele num: 656
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 1.768e0

DP
type: SiteQuality
SIO_000300: 1.23641e5

QD
type: SiteQuality
SIO_000300: 1.204e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.44e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.256281407035176e-3
allele num: 796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2666
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.531e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.598e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.218e0

DP
type: SiteQuality
SIO_000300: 1.34568e5

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 1.207729468599034e-3
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

DP
type: SiteQuality
SIO_000300: 1.3572e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 1.538461538461539e-2
allele num: 130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.22e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.36853e5

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.27e-1

FS
type: SiteQuality
SIO_000300: 2.369e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

GenotypeQuality
all individuals: 125
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.428571428571429e-3
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3766
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.74043e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

GenotypeQuality
all individuals: 202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.847953216374269e-4
allele num: 1710
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.09e-1

FS
type: SiteQuality
SIO_000300: 2.276e0

MQ
type: SiteQuality
SIO_000300: 5.762e1

VQSLOD
type: SiteQuality
SIO_000300: -1.276e0

QD
type: SiteQuality
SIO_000300: 1.282e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.79125e5

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

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.36630383341221e-4
allele num: 4226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.805e0

MQ
type: SiteQuality
SIO_000300: 5.361e1

FS
type: SiteQuality
SIO_000300: 8.179999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.9749e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 2.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.195e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.398e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.35e0

GenotypeQuality
all individuals: 2360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1658
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.174603174603175e-3
allele num: 630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

QD
type: SiteQuality
SIO_000300: 1.369e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.25e0

VQSLOD
type: SiteQuality
SIO_000300: -2.316e-1

FS
type: SiteQuality
SIO_000300: 2.41e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
type: SiteQuality
SIO_000300: 2.04552e5

MQRankSum
type: SiteQuality
SIO_000300: -1.213e0

GenotypeQuality
all individuals: 529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
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variant carriers: 1

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 197
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GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 4898
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variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.330494944119212e-4
allele num: 7516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1630
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 8.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.621e0

VQSLOD
type: SiteQuality
SIO_000300: -8.683999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.03e-2

DP
type: SiteQuality
SIO_000300: 2.09212e5

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 530
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GenotypeQuality
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GenotypeQuality
all individuals: 741
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.431906614785992e-4
allele num: 4112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

DP
type: SiteQuality
SIO_000300: 2.0928e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.98e-2

FS
type: SiteQuality
SIO_000300: 2.171e0

QD
type: SiteQuality
SIO_000300: 1.373e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.044e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 77
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.428e0

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.09e-2

FS
type: SiteQuality
SIO_000300: 4.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

QD
type: SiteQuality
SIO_000300: 1.064e1

DP
type: SiteQuality
SIO_000300: 2.11539e5

GenotypeQuality
all individuals: 130
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 4938
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.344481605351171e-3
allele num: 598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 3.360537686029765e-3
allele num: 4166
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 1.5625e-2
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.165228113440197e-4
allele num: 1622
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.595744680851064e-2
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 122
allele frequency: 1.604840831360168e-2
allele num: 7602
num of homozygotes: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

DP
type: SiteQuality
SIO_000300: 2.18154e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

GenotypeQuality
all individuals: 760
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 242
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.75e1
variant carriers: 1

African
type: Population
allele count: 2
allele frequency: 3.322259136212625e-3
allele num: 602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.208333333333333e-3
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4168
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.04e0

QD
type: SiteQuality
SIO_000300: 1.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.36e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.13735e5

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4970
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.324152542372881e-4
allele num: 7552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 9.779999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

DP
type: SiteQuality
SIO_000300: 2.10301e5

VQSLOD
type: SiteQuality
SIO_000300: -6.501e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

GenotypeQuality
all individuals: 557
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 52
allele frequency: 6.887417218543046e-3
allele num: 7550
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

FS
type: SiteQuality
SIO_000300: 3.789e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 2.10962e5

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.327668613913967e-4
allele num: 7532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4086
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1612
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.398e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: -1.432e0

DP
type: SiteQuality
SIO_000300: 2.09532e5

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 496
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 9.75e1
variant carriers: 7

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.219512195121951e-2
allele num: 574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3946
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.03624e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.574e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 9.75e1
variant carriers: 20

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

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.211047420531526e-4
allele num: 3838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 2.992957746478873e-2
allele num: 568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 1.98054e5

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.45e-1

GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3098
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.829491401390413e-4
allele num: 5466
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.59015e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

VQSLOD
type: SiteQuality
SIO_000300: -1.876e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.165e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQ
type: SiteQuality
SIO_000300: 5.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 539
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 6.25e1
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GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.53e-2

QD
type: SiteQuality
SIO_000300: 1.257e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
SIO_000300: 9.6605e4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-1

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

GenotypeQuality
all individuals: 401
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 1363
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variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 904
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 470
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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: 1.527323823196994e-5
allele num: 65474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.771e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-1

FS
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 8.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

DP
type: SiteQuality
SIO_000300: 1.995428e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

VQSLOD
type: SiteQuality
SIO_000300: -2.645e0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65468
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: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.996734e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

FS
type: SiteQuality
SIO_000300: 6.615e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.571e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.27e-1

QD
type: SiteQuality
SIO_000300: 3.99e0

VQSLOD
type: SiteQuality
SIO_000300: -2.793e-1

GenotypeQuality
all individuals: 3401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
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: 0
allele frequency: 0.0e0
allele num: 65750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.02388180530257e-4
allele num: 9882
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.844e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.816e1

FS
type: SiteQuality
SIO_000300: 3.053e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 2.019746e6

VQSLOD
type: SiteQuality
SIO_000300: -9.971e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
all individuals: 8384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 37232
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66112
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.405578869414959e-4
allele num: 16204
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: 10190
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.081e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.776e0

QD
type: SiteQuality
SIO_000300: 1.095e1

FS
type: SiteQuality
SIO_000300: 2.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

DP
type: SiteQuality
SIO_000300: 2.037639e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

MQ
type: SiteQuality
SIO_000300: 5.677e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 37549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 8.25e1
variant carriers: 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: 10242
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66222
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.125949522175937e-5
allele num: 16324
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.574e1

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

MQ
type: SiteQuality
SIO_000300: 5.533e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

DP
type: SiteQuality
SIO_000300: 2.041676e6

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.648e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 215
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8470
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
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: 8646
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.818e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.253e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

FS
type: SiteQuality
SIO_000300: 1.136e0

MQ
type: SiteQuality
SIO_000300: 5.727e1

DP
type: SiteQuality
SIO_000300: 2.050129e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.244482173174873e-4
allele num: 16492
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 2.051557e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.302e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.781e1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
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

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

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

MQ
type: SiteQuality
SIO_000300: 5.668e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.05101e6

FS
type: SiteQuality
SIO_000300: 5.19e-1

BaseQRankSum
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SIO_000300: -3.905e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1234
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GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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MQ
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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InbreedingCoeff
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QD
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MQ
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Other
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Latino
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European (Non-Finnish)
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African
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South Asian
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DP
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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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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FS
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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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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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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South Asian
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African
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.218e0

DP
type: SiteQuality
SIO_000300: 2.04868e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

European (Finnish)
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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: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507749834147518e-5
allele num: 66324
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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SIO_000300: -8.6e-1

MQRankSum
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SIO_000300: 7.89e-1

BaseQRankSum
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SIO_000300: 3.5e0

FS
type: SiteQuality
SIO_000300: 7.49e-1

DP
type: SiteQuality
SIO_000300: 2.044662e6

MQ
type: SiteQuality
SIO_000300: 5.102e1

QD
type: SiteQuality
SIO_000300: 1.041e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.043947e6

InbreedingCoeff
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VQSLOD
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 5.793e1

ReadPosRankSum
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SIO_000300: 6.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512310205069264e-5
allele num: 66124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 7.701e0

MQ
type: SiteQuality
SIO_000300: 5.582e1

ClippingRankSum
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SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.892e0

VQSLOD
type: SiteQuality
SIO_000300: -1.507e0

DP
type: SiteQuality
SIO_000300: 2.039232e6

QD
type: SiteQuality
SIO_000300: 1.456e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
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: 906
num of homozygotes: 0

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

South Asian
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allele frequency: 1.212268153715602e-4
allele num: 16498
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 66170
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
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SIO_000300: -3.9e-1

ClippingRankSum
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FS
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QD
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MQ
type: SiteQuality
SIO_000300: 5.65e1

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

BaseQRankSum
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SIO_000300: -2.432e0

DP
type: SiteQuality
SIO_000300: 2.036434e6

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
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allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66032
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

DP
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MQ
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 1.892e0

InbreedingCoeff
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SIO_000300: 2.0e-3

ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521375323292256e-5
allele num: 65730
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

Latino
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allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.723e1

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

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

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

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.528677999266235e-5
allele num: 65416
num of homozygotes: 0

QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535060788407221e-5
allele num: 65144
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.693e1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

MQ
type: SiteQuality
SIO_000300: 5.868e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

DP
type: SiteQuality
SIO_000300: 1.965606e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.069999999999999e-2

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 41

GenotypeQuality
all individuals: 1506
bin: 8.25e1
variant carriers: 73

GenotypeQuality
all individuals: 5566
bin: 6.75e1
variant carriers: 56

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 104

GenotypeQuality
all individuals: 2051
bin: 2.25e1
variant carriers: 14

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 309
bin: 5.25e1
variant carriers: 23

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 9

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 18

GenotypeQuality
all individuals: 17267
bin: 9.75e1
variant carriers: 15213

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 48

GenotypeQuality
all individuals: 857
bin: 9.25e1
variant carriers: 90

GenotypeQuality
all individuals: 2497
bin: 7.75e1
variant carriers: 83

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 11

GenotypeQuality
all individuals: 25798
bin: 6.25e1
variant carriers: 57

African
type: Population
allele count: 2986
allele frequency: 2.925156739811912e-1
allele num: 10208
num of homozygotes: 426

European (Finnish)
type: Population
allele count: 538
allele frequency: 8.158932362754019e-2
allele num: 6594
num of homozygotes: 22

South Asian
type: Population
allele count: 3595
allele frequency: 2.223527956457199e-1
allele num: 16168
num of homozygotes: 407

East Asian
type: Population
allele count: 2725
allele frequency: 3.227908078654347e-1
allele num: 8442
num of homozygotes: 406

Latino
type: Population
allele count: 3301
allele frequency: 2.888013998250219e-1
allele num: 11430
num of homozygotes: 499

European (Non-Finnish)
type: Population
allele count: 4583
allele frequency: 7.035183593270293e-2
allele num: 65144
num of homozygotes: 180

Other
type: Population
allele count: 102
allele frequency: 1.140939597315436e-1
allele num: 894
num of homozygotes: 6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.069999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 1.965606e6

MQ
type: SiteQuality
SIO_000300: 5.868e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.693e1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

GenotypeQuality
all individuals: 142
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2999
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3062
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2503
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34798
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.165608237252604e-5
allele num: 64876
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15944
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.045e0

QD
type: SiteQuality
SIO_000300: 1.521e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.67987e6

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.201e-1

MQ
type: SiteQuality
SIO_000300: 5.806e1

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543733983759918e-5
allele num: 64778
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.805999999999999e0

DP
type: SiteQuality
SIO_000300: 1.670284e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.028e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 5.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.587e0

MQ
type: SiteQuality
SIO_000300: 5.707e1