6-154535307-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535307
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535307
    reference: chr 6
allele count: 1
allele frequency: 8.340561820244212e-6
allele num: 119896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32520T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32520T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+45A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+45A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-154535314-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535314
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535314
    reference: chr 6
allele count: 1
allele frequency: 8.334027835652971e-6
allele num: 119990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32513T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32513T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+38A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+38A>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

6-154535321-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535321
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535321
    reference: chr 6
allele count: 2
allele frequency: 1.664641353020492e-5
allele num: 120146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32506T>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+31A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32506T>A
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16251
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

6-154535324-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535324
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535324
    reference: chr 6
allele count: 1
allele frequency: 8.316008316008316e-6
allele num: 120250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32503A>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+28T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32503A>T
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13566
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-154535341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535341
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535341
    reference: chr 6
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32486A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32486A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+11T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+11T>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

6-154535345-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535345
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535345
    reference: chr 6
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32482A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+7T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32482A>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.75e1
  variant carriers: 0
hgvs: c.451+7T>C
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-154535349-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535349
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535349
    reference: chr 6
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.364+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.448+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.203+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.364+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.451+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.364+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32478T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32478T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.96+3A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.451+3A>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: c.451+3A>C
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-154535354-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535354
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535354
    reference: chr 6
allele count: 2
allele frequency: 1.65180046250413e-5
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.362A>G
  hgvsp: ENSP00000428767.1:p.Glu121Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32473T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32473T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.362A>G
  hgvsp: ENSP00000431092.1:p.Glu121Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.94A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.362A>G
  hgvsp: ENSP00000430287.1:p.Glu121Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.446A>G
  hgvsp: ENSP00000265198.4:p.Glu149Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.449A>G
  hgvsp: ENSP00000356189.4:p.Glu150Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.449A>G
  hgvsp: ENSP00000394751.2:p.Glu150Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.201A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10642
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu150Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-154535366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535366
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535366
    reference: chr 6
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.350C>T
  hgvsp: ENSP00000430287.1:p.Thr117Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32461G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.82C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32461G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.350C>T
  hgvsp: ENSP00000428767.1:p.Thr117Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.437C>T
  hgvsp: ENSP00000394751.2:p.Thr146Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.434C>T
  hgvsp: ENSP00000265198.4:p.Thr145Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.350C>T
  hgvsp: ENSP00000431092.1:p.Thr117Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.189C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.437C>T
  hgvsp: ENSP00000356189.4:p.Thr146Ile
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21730
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr146Ile
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

6-154535367-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535367
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535367
    reference: chr 6
allele count: 3
allele frequency: 2.475002475002475e-5
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.349A>T
  hgvsp: ENSP00000431092.1:p.Thr117Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.436A>T
  hgvsp: ENSP00000356189.4:p.Thr146Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.349A>T
  hgvsp: ENSP00000428767.1:p.Thr117Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.436A>T
  hgvsp: ENSP00000394751.2:p.Thr146Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.349A>T
  hgvsp: ENSP00000430287.1:p.Thr117Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.433A>T
  hgvsp: ENSP00000265198.4:p.Thr145Ser
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32460T>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.81A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32460T>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.188A>T
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr146Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

6-154535373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535373
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535373
    reference: chr 6
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.343G>A
  hgvsp: ENSP00000428767.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.182G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.430G>A
  hgvsp: ENSP00000394751.2:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.343G>A
  hgvsp: ENSP00000430287.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32454C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32454C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.75G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.343G>A
  hgvsp: ENSP00000431092.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.427G>A
  hgvsp: ENSP00000265198.4:p.Glu143Lys
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.430G>A
  hgvsp: ENSP00000356189.4:p.Glu144Lys
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3483
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4185
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu144Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-154535378-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535378
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535378
    reference: chr 6
allele count: 2
allele frequency: 1.649620587264929e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.70A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.177A>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32449T>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.422A>T
  hgvsp: ENSP00000265198.4:p.His141Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.338A>T
  hgvsp: ENSP00000430287.1:p.His113Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.338A>T
  hgvsp: ENSP00000431092.1:p.His113Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.338A>T
  hgvsp: ENSP00000428767.1:p.His113Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.425A>T
  hgvsp: ENSP00000394751.2:p.His142Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32449T>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.425A>T
  hgvsp: ENSP00000356189.4:p.His142Leu
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His142Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

6-154535382-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535382
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535382
    reference: chr 6
allele count: 3
allele frequency: 2.474145182839329e-5
allele num: 121254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.334A>C
  hgvsp: ENSP00000431092.1:p.Ile112Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.421A>C
  hgvsp: ENSP00000394751.2:p.Ile141Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.418A>C
  hgvsp: ENSP00000265198.4:p.Ile140Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.334A>C
  hgvsp: ENSP00000428767.1:p.Ile112Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.66A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32445T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.421A>C
  hgvsp: ENSP00000356189.4:p.Ile141Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.173A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.334A>C
  hgvsp: ENSP00000430287.1:p.Ile112Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32445T>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile141Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-154535384-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535384
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535384
    reference: chr 6
allele count: 5
allele frequency: 4.125412541254125e-5
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.332T>G
  hgvsp: ENSP00000431092.1:p.Val111Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.332T>G
  hgvsp: ENSP00000428767.1:p.Val111Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.416T>G
  hgvsp: ENSP00000265198.4:p.Val139Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32443A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.332T>G
  hgvsp: ENSP00000430287.1:p.Val111Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.419T>G
  hgvsp: ENSP00000356189.4:p.Val140Gly
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.171T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.64T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32443A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.419T>G
  hgvsp: ENSP00000394751.2:p.Val140Gly
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 17501
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val140Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-154535385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535385
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535385
    reference: chr 6
allele count: 3
allele frequency: 2.474185992808366e-5
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.170G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.63G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32442C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32442C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.418G>A
  hgvsp: ENSP00000394751.2:p.Val140Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.331G>A
  hgvsp: ENSP00000430287.1:p.Val111Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.418G>A
  hgvsp: ENSP00000356189.4:p.Val140Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.331G>A
  hgvsp: ENSP00000428767.1:p.Val111Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.415G>A
  hgvsp: ENSP00000265198.4:p.Val139Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.331G>A
  hgvsp: ENSP00000431092.1:p.Val111Ile
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val140Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

6-154535388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535388
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535388
    reference: chr 6
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.415G>A
  hgvsp: ENSP00000356189.4:p.Ala139Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.412G>A
  hgvsp: ENSP00000265198.4:p.Ala138Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.328G>A
  hgvsp: ENSP00000430287.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.328G>A
  hgvsp: ENSP00000431092.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32439C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.328G>A
  hgvsp: ENSP00000428767.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32439C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.167G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.415G>A
  hgvsp: ENSP00000394751.2:p.Ala139Thr
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.60G>A
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala139Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-154535389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535389
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535389
    reference: chr 6
allele count: 6
allele frequency: 4.948290365678658e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.327G>A
  hgvsp: ENST00000517438.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.59G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.414G>A
  hgvsp: ENST00000422970.2:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.411G>A
  hgvsp: ENST00000265198.4:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.166G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.327G>A
  hgvsp: ENST00000519344.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.327G>A
  hgvsp: ENST00000519405.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.414G>A
  hgvsp: ENST00000367220.4:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32438C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32438C>T
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser138Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

6-154535390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535390
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535390
    reference: chr 6
allele count: 19
allele frequency: 1.566984462111965e-4
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32437G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.326C>T
  hgvsp: ENSP00000428767.1:p.Ser109Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.326C>T
  hgvsp: ENSP00000430287.1:p.Ser109Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.413C>T
  hgvsp: ENSP00000394751.2:p.Ser138Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.165C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.413C>T
  hgvsp: ENSP00000356189.4:p.Ser138Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.410C>T
  hgvsp: ENSP00000265198.4:p.Ser137Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.326C>T
  hgvsp: ENSP00000431092.1:p.Ser109Leu
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32437G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.58C>T
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser138Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

6-154535390-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535390
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535390
    reference: chr 6
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.413C>G
  hgvsp: ENSP00000356189.4:p.Ser138Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.326C>G
  hgvsp: ENSP00000430287.1:p.Ser109Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32437G>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.410C>G
  hgvsp: ENSP00000265198.4:p.Ser137Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.165C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.326C>G
  hgvsp: ENSP00000428767.1:p.Ser109Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.326C>G
  hgvsp: ENSP00000431092.1:p.Ser109Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.58C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.413C>G
  hgvsp: ENSP00000394751.2:p.Ser138Trp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32437G>C
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser138Trp
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-154535393-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535393
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535393
    reference: chr 6
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.407G>T
  hgvsp: ENSP00000265198.4:p.Gly136Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.410G>T
  hgvsp: ENSP00000394751.2:p.Gly137Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.410G>T
  hgvsp: ENSP00000356189.4:p.Gly137Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32434C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.323G>T
  hgvsp: ENSP00000429972.1:p.Gly108Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32434C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.323G>T
  hgvsp: ENSP00000428767.1:p.Gly108Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.55G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.162G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.323G>T
  hgvsp: ENSP00000430287.1:p.Gly108Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.323G>T
  hgvsp: ENSP00000431092.1:p.Gly108Val
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly137Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-154535403-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535403
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535403
    reference: chr 6
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.313A>G
  hgvsp: ENSP00000428767.1:p.Asn105Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.400A>G
  hgvsp: ENSP00000356189.4:p.Asn134Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.313A>G
  hgvsp: ENSP00000430287.1:p.Asn105Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32424T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.313A>G
  hgvsp: ENSP00000429972.1:p.Asn105Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.397A>G
  hgvsp: ENSP00000265198.4:p.Asn133Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32424T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.152A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.400A>G
  hgvsp: ENSP00000394751.2:p.Asn134Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.313A>G
  hgvsp: ENSP00000431092.1:p.Asn105Asp
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.45A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn134Asp
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-154535417-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535417
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535417
    reference: chr 6
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.31A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-7A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32410T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32410T>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.393-7A>C
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

6-154535424-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535424
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535424
    reference: chr 6
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32403A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32403A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.24T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-14T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-14T>C
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6526
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21274
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-154535427-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535427
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535427
    reference: chr 6
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.21T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32400A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-17T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32400A>G
  variant of: http://identifiers.org/hgnc/8156
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/6-154535428-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535428
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535428
    reference: chr 6
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32399A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.20T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32399A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-18T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-18T>G
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-154535434-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535434
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535434
    reference: chr 6
allele count: 6
allele frequency: 4.954501164307774e-5
allele num: 121102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32393T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.14A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32393T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-24A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-24A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20292
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

6-154535438-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535438
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535438
    reference: chr 6
allele count: 6
allele frequency: 4.955728822518832e-5
allele num: 121072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.10C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32389G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-28C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32389G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-28C>T
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-154535444-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535444
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535444
    reference: chr 6
allele count: 19644
allele frequency: 1.624840774868071e-1
allele num: 120898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32383A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.4T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-34T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32383A>G
  variant of: http://identifiers.org/hgnc/8156
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 272
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 3.75e1
  variant carriers: 2302
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11514
  bin: 2.75e1
  variant carriers: 1202
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 494
genotype depth: GenotypeDepth
  all individuals: 11189
  bin: 2.25e1
  variant carriers: 660
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 633
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.75e1
  variant carriers: 739
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 4.25e1
  variant carriers: 2361
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.75e1
  variant carriers: 1350
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 2245
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.75e1
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.75e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 5.25e1
  variant carriers: 1808
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 3.25e1
  variant carriers: 1813
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 6.25e1
  variant carriers: 1024
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 7
num of homozygotes: 1705
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

6-154535447-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535447
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535447
    reference: chr 6
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000484827
  gene symbol: IPCEF1
  hgvsc: ENST00000484827.1:n.1C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32380G>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32380G>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-37C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-37C>G
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS

6-154535453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535453
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535453
    reference: chr 6
allele count: 20
allele frequency: 1.656863557286057e-4
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32374C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32374C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-43G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-43G>A
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12987
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

6-154535457-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535457
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535457
    reference: chr 6
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32370C>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-47G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32370C>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/6-154535457-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535457
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535457
    reference: chr 6
allele count: 3
allele frequency: 2.485954357877989e-5
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32370C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32370C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-47G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-47G>T
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6708
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13159
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD

6-154535458-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154535458
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154535458
    reference: chr 6
allele count: 83
allele frequency: 6.881684769090456e-4
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.306-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.393-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-32369C>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.306-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.393-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.306-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.390-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000519091
  gene symbol: IPCEF1
  hgvsc: ENST00000519091.1:n.145-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.306-48G>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-32369C>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10476
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12692
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

6-154542354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542354
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542354
    reference: chr 6
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25473C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+37G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25473C>T
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

6-154542357-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542357
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542357
    reference: chr 6
allele count: 12
allele frequency: 9.951403977244456e-5
allele num: 120586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25470T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25470T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+34A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+34A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19830
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20321
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

6-154542360-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542360
    reference: chr 6
allele count: 50
allele frequency: 4.144562334217507e-4
allele num: 120640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25467A>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25467A>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+31T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+31T>A
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 20603
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20499
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-154542368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542368
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542368
    reference: chr 6
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+23C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25459G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25459G>A
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

6-154542368-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542368
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542368
    reference: chr 6
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25459G>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+23C>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25459G>C
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
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: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

6-154542371-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542371
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542371
    reference: chr 6
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25456T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+20A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25456T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+20A>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-154542381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542381
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542381
    reference: chr 6
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.389+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.392+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.305+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.305+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.305+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25446C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25446C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.305+10G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.392+10G>A
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8014
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6677
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7474
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-154542392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542392
    reference: chr 6
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25435C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.304G>A
  hgvsp: ENSP00000429972.1:p.Val102Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.304G>A
  hgvsp: ENSP00000430287.1:p.Val102Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.391G>A
  hgvsp: ENSP00000394751.2:p.Val131Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.304G>A
  hgvsp: ENSP00000428767.1:p.Val102Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25435C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.304G>A
  hgvsp: ENSP00000431092.1:p.Val102Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.388G>A
  hgvsp: ENSP00000265198.4:p.Val130Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.391G>A
  hgvsp: ENSP00000356189.4:p.Val131Met
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37435
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6678
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val131Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-154542393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542393
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542393
    reference: chr 6
allele count: 2
allele frequency: 1.651391297167864e-5
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.390C>T
  hgvsp: ENST00000422970.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.303C>T
  hgvsp: ENST00000519405.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.303C>T
  hgvsp: ENST00000519190.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.303C>T
  hgvsp: ENST00000519344.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.387C>T
  hgvsp: ENST00000265198.4:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25434G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.390C>T
  hgvsp: ENST00000367220.4:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25434G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.303C>T
  hgvsp: ENST00000517438.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21069
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
hgvs: c.390C>T
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD

6-154542402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542402
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542402
    reference: chr 6
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25425C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25425C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.294G>A
  hgvsp: ENST00000519405.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.294G>A
  hgvsp: ENST00000519344.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.294G>A
  hgvsp: ENST00000519190.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.294G>A
  hgvsp: ENST00000517438.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.381G>A
  hgvsp: ENST00000422970.2:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.378G>A
  hgvsp: ENST00000265198.4:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.381G>A
  hgvsp: ENST00000367220.4:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln127Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

6-154542435-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542435
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542435
    reference: chr 6
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.348C>G
  hgvsp: ENSP00000356189.4:p.Ile116Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.261C>G
  hgvsp: ENSP00000431092.1:p.Ile87Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.345C>G
  hgvsp: ENSP00000265198.4:p.Ile115Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.348C>G
  hgvsp: ENSP00000394751.2:p.Ile116Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.261C>G
  hgvsp: ENSP00000430287.1:p.Ile87Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.261C>G
  hgvsp: ENSP00000429972.1:p.Ile87Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25392G>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.261C>G
  hgvsp: ENSP00000428767.1:p.Ile87Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25392G>C
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile116Met
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-154542447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542447
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542447
    reference: chr 6
allele count: 2
allele frequency: 1.654478673769895e-5
allele num: 120884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.249C>T
  hgvsp: ENST00000519190.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.249C>T
  hgvsp: ENST00000517438.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.333C>T
  hgvsp: ENST00000265198.4:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.249C>T
  hgvsp: ENST00000519344.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.336C>T
  hgvsp: ENST00000422970.2:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25380G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.249C>T
  hgvsp: ENST00000519405.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25380G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.336C>T
  hgvsp: ENST00000367220.4:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser112Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

6-154542452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542452
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542452
    reference: chr 6
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.244A>G
  hgvsp: ENSP00000430287.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.244A>G
  hgvsp: ENSP00000429972.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25375T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.244A>G
  hgvsp: ENSP00000428767.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.331A>G
  hgvsp: ENSP00000356189.4:p.Ile111Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.244A>G
  hgvsp: ENSP00000431092.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.331A>G
  hgvsp: ENSP00000394751.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.328A>G
  hgvsp: ENSP00000265198.4:p.Ile110Val
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25375T>C
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile111Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/6-154542462-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542462
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542462
    reference: chr 6
allele count: 1
allele frequency: 8.315870006320061e-6
allele num: 120252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318T>G
  hgvsp: ENSP00000265198.4:p.His106Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234T>G
  hgvsp: ENSP00000429972.1:p.His78Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25365A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234T>G
  hgvsp: ENSP00000428767.1:p.His78Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25365A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234T>G
  hgvsp: ENSP00000430287.1:p.His78Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321T>G
  hgvsp: ENSP00000356189.4:p.His107Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321T>G
  hgvsp: ENSP00000394751.2:p.His107Gln
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234T>G
  hgvsp: ENSP00000431092.1:p.His78Gln
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His107Gln
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-154542477-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542477
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542477
    reference: chr 6
allele count: 3
allele frequency: 2.522958926228681e-5
allele num: 118908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-15T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25350A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25350A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-15T>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19904
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6665
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/6-154542486-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542486
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542486
    reference: chr 6
allele count: 1
allele frequency: 8.481188723411473e-6
allele num: 117908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25341A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25341A>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-24T>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-24T>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6756
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2495
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

6-154542491-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542491
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542491
    reference: chr 6
allele count: 19183
allele frequency: 1.641845974768483e-1
allele num: 116838
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-29T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25336A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25336A>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 427
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.25e1
  variant carriers: 3208
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.75e1
  variant carriers: 743
genotype depth: GenotypeDepth
  all individuals: 9438
  bin: 1.25e1
  variant carriers: 787
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 3.75e1
  variant carriers: 1509
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 14101
  bin: 2.75e1
  variant carriers: 3214
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 4.25e1
  variant carriers: 1043
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 3.25e1
  variant carriers: 2419
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 1.75e1
  variant carriers: 2092
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 541
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 9.75e1
  variant carriers: 749
genotype quality: GenotypeQuality
  all individuals: 3209
  bin: 6.75e1
  variant carriers: 120
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 4.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 15964
  bin: 6.25e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 2.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 3.25e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 19950
  bin: 9.75e1
  variant carriers: 16449
num of homozygotes: 1629
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

6-154542495-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542495
    reference: chr 6
allele count: 1
allele frequency: 8.636473555117974e-6
allele num: 115788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25332A>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-33T>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25332A>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-33T>A
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16518
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1615
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-154542503-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542503
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542503
    reference: chr 6
allele count: 1
allele frequency: 8.732404205525866e-6
allele num: 114516
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25324T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-41A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25324T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-41A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7433
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13217
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-154542506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154542506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154542506
    reference: chr 6
allele count: 19
allele frequency: 1.673831841567411e-4
allele num: 113512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.234-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.321-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.234-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.234-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.318-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-25321T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-25321T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.321-44A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.234-44A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7802
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3970
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8257
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-154544258-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544258
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544258
    reference: chr 6
allele count: 1
allele frequency: 8.573094201159083e-6
allele num: 116644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.233+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.320+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.233+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23569A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.317+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.233+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.320+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.422T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.233+46T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23569A>G
  variant of: http://identifiers.org/hgnc/8156
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11243
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

6-154544287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544287
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544287
    reference: chr 6
allele count: 1
allele frequency: 8.491126772522713e-6
allele num: 117770
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.320+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.393C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.317+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23540G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.233+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.320+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.233+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23540G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.233+17C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.233+17C>T
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-154544289-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544289
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544289
    reference: chr 6
allele count: 1
allele frequency: 8.478456242687331e-6
allele num: 117946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.233+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.320+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.233+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.233+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.391A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23538T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.233+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.317+15A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23538T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.320+15A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5101
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-154544304-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544304
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544304
    reference: chr 6
allele count: 1
allele frequency: 8.426445556735258e-6
allele num: 118674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.233A>C
  hgvsp: ENSP00000428767.1:p.His78Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.233A>C
  hgvsp: ENSP00000430287.1:p.His78Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.320A>C
  hgvsp: ENSP00000394751.2:p.His107Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.320A>C
  hgvsp: ENSP00000356189.4:p.His107Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.233A>C
  hgvsp: ENSP00000431092.1:p.His78Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23523T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.233A>C
  hgvsp: ENSP00000429972.1:p.His78Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.317A>C
  hgvsp: ENSP00000265198.4:p.His106Pro
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.376A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23523T>G
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32380
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His107Pro
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

6-154544306-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544306
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544306
    reference: chr 6
allele count: 1
allele frequency: 8.42133629764371e-6
allele num: 118746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23521C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.231G>A
  hgvsp: ENST00000519405.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.231G>A
  hgvsp: ENST00000519344.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.318G>A
  hgvsp: ENST00000367220.4:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.231G>A
  hgvsp: ENST00000519190.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.315G>A
  hgvsp: ENST00000265198.4:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.231G>A
  hgvsp: ENST00000517438.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.374G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23521C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.318G>A
  hgvsp: ENST00000422970.2:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.318G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

6-154544322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544322
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544322
    reference: chr 6
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.215C>T
  hgvsp: ENSP00000428767.1:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.302C>T
  hgvsp: ENSP00000356189.4:p.Ser101Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.215C>T
  hgvsp: ENSP00000429972.1:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23505G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.215C>T
  hgvsp: ENSP00000431092.1:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.299C>T
  hgvsp: ENSP00000265198.4:p.Ser100Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.215C>T
  hgvsp: ENSP00000430287.1:p.Ser72Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.358C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.302C>T
  hgvsp: ENSP00000394751.2:p.Ser101Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23505G>A
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser101Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS

6-154544324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544324
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544324
    reference: chr 6
allele count: 1
allele frequency: 8.415808254224735e-6
allele num: 118824
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.300A>G
  hgvsp: ENST00000422970.2:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.297A>G
  hgvsp: ENST00000265198.4:c.297A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.213A>G
  hgvsp: ENST00000517438.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.213A>G
  hgvsp: ENST00000519190.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.213A>G
  hgvsp: ENST00000519405.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.300A>G
  hgvsp: ENST00000367220.4:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23503T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23503T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.213A>G
  hgvsp: ENST00000519344.1:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.356A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala100Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

6-154544335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544335
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544335
    reference: chr 6
allele count: 2
allele frequency: 1.691274713751755e-5
allele num: 118254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.202G>A
  hgvsp: ENSP00000430287.1:p.Val68Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.202G>A
  hgvsp: ENSP00000428767.1:p.Val68Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.202G>A
  hgvsp: ENSP00000429972.1:p.Val68Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.289G>A
  hgvsp: ENSP00000394751.2:p.Val97Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.345G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.286G>A
  hgvsp: ENSP00000265198.4:p.Val96Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.289G>A
  hgvsp: ENSP00000356189.4:p.Val97Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.202G>A
  hgvsp: ENSP00000431092.1:p.Val68Met
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23492C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23492C>T
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val97Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/6-154544356-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544356
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544356
    reference: chr 6
allele count: 1
allele frequency: 8.674230595746157e-6
allele num: 115284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.265G>T
  hgvsp: ENSP00000265198.4:p.Val89Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23471C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.181G>T
  hgvsp: ENSP00000431092.1:p.Val61Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.181G>T
  hgvsp: ENSP00000428767.1:p.Val61Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.181G>T
  hgvsp: ENSP00000429972.1:p.Val61Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.268G>T
  hgvsp: ENSP00000394751.2:p.Val90Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.181G>T
  hgvsp: ENSP00000430287.1:p.Val61Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.268G>T
  hgvsp: ENSP00000356189.4:p.Val90Phe
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.324G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23471C>A
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val90Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

6-154544356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544356
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544356
    reference: chr 6
allele count: 1
allele frequency: 8.674230595746157e-6
allele num: 115284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.268G>A
  hgvsp: ENSP00000394751.2:p.Val90Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23471C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.268G>A
  hgvsp: ENSP00000356189.4:p.Val90Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.265G>A
  hgvsp: ENSP00000265198.4:p.Val89Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.181G>A
  hgvsp: ENSP00000428767.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.324G>A
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.181G>A
  hgvsp: ENSP00000430287.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.181G>A
  hgvsp: ENSP00000429972.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23471C>T
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.181G>A
  hgvsp: ENSP00000431092.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val90Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-154544360-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544360
    reference: chr 6
allele count: 1
allele frequency: 8.749365670988854e-6
allele num: 114294
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.264A>C
  hgvsp: ENST00000422970.2:c.264A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.177A>C
  hgvsp: ENST00000519405.1:c.177A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23467T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.264A>C
  hgvsp: ENST00000367220.4:c.264A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.177A>C
  hgvsp: ENST00000519190.1:c.177A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.177A>C
  hgvsp: ENST00000519344.1:c.177A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.261A>C
  hgvsp: ENST00000265198.4:c.261A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.320A>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23467T>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.177A>C
  hgvsp: ENST00000517438.1:c.177A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly88Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

6-154544380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544380
    reference: chr 6
allele count: 1
allele frequency: 9.381391072668256e-6
allele num: 106594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.160-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.247-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23447G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.244-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23447G>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.160-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.303-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.160-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.247-3C>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.160-3C>T
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
hgvs: c.247-3C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-154544384-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544384
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544384
    reference: chr 6
allele count: 1
allele frequency: 9.533615528352973e-6
allele num: 104892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.247-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.160-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.244-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23443C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.160-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.160-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23443C>A
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.247-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.160-7G>T
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.303-7G>T
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
hgvs: c.247-7G>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

6-154544386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544386
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544386
    reference: chr 6
allele count: 4
allele frequency: 3.836120914531226e-5
allele num: 104272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.160-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.247-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.160-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23441A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.303-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23441A>G
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.247-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.160-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.160-9T>C
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.244-9T>C
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13444
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10516
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5094
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-154544388-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544388
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544388
    reference: chr 6
allele count: 1
allele frequency: 9.628345850182938e-6
allele num: 103860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23439T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.247-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.160-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.160-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23439T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.247-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.303-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.244-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.160-11A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.160-11A>G
  variant of: http://identifiers.org/hgnc/21204
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

6-154544390-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154544390
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 154544390
    reference: chr 6
allele count: 1
allele frequency: 9.682416731216111e-6
allele num: 103280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000431092
  ensembl transcript: ENST00000517438
  gene symbol: IPCEF1
  hgvsc: ENST00000517438.1:c.160-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000430287
  ensembl transcript: ENST00000519344
  gene symbol: IPCEF1
  hgvsc: ENST00000519344.1:c.160-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000265198
  ensembl transcript: ENST00000265198
  gene symbol: IPCEF1
  hgvsc: ENST00000265198.4:c.244-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000338381
  ensembl transcript: ENST00000337049
  gene symbol: OPRM1
  hgvsc: ENST00000337049.4:c.1165-23437T>C
  variant of: http://identifiers.org/hgnc/8156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000394751
  ensembl transcript: ENST00000422970
  gene symbol: IPCEF1
  hgvsc: ENST00000422970.2:c.247-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl transcript: ENST00000518162
  gene symbol: IPCEF1
  hgvsc: ENST00000518162.1:n.303-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000429972
  ensembl transcript: ENST00000519190
  gene symbol: IPCEF1
  hgvsc: ENST00000519190.1:c.160-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000428767
  ensembl transcript: ENST00000519405
  gene symbol: IPCEF1
  hgvsc: ENST00000519405.1:c.160-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000074706
  ensembl protein: ENSP00000356189
  ensembl transcript: ENST00000367220
  gene symbol: IPCEF1
  hgvsc: ENST00000367220.4:c.247-13A>G
  variant of: http://identifiers.org/hgnc/21204
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112038
  ensembl protein: ENSP00000430575
  ensembl transcript: ENST00000524150
  gene symbol: OPRM1
  hgvsc: ENST00000524150.2:c.*251-23437T>C
  variant of: http://identifiers.org/hgnc/8156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9538
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3934
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4922
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13542
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2951
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519248883352071e-5
allele num: 65822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.644e1

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

DP
type: SiteQuality
SIO_000300: 1.935648e6

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

FS
type: SiteQuality
SIO_000300: 3.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13553
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 924
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3359
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2974
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4112
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6888
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.033e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.957588e6

QD
type: SiteQuality
SIO_000300: 1.654e1

GenotypeQuality
all individuals: 585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 641
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13566
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5036
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7025
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215953307392996e-4
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.094e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.92e-1

DP
type: SiteQuality
SIO_000300: 1.978565e6

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.373e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 19681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5059
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2162
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51372952680815e-5
allele num: 66062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.587e0

DP
type: SiteQuality
SIO_000300: 1.984593e6

QD
type: SiteQuality
SIO_000300: 1.516e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: -4.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

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

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

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

GenotypeQuality
all individuals: 2999
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13573
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

FS
type: SiteQuality
SIO_000300: 2.607e0

DP
type: SiteQuality
SIO_000300: 2.002733e6

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.332e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21466
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3480
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

DP
type: SiteQuality
SIO_000300: 2.004593e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.068e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.368e0

GenotypeQuality
all individuals: 3485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
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

MQRankSum
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SIO_000300: 1.65e0

MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.64e0

FS
type: SiteQuality
SIO_000300: 2.108e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

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

South Asian
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allele frequency: 0.0e0
allele num: 16494
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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00318337437684e-5
allele num: 66596
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

FS
type: SiteQuality
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MQRankSum
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MQ
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SIO_000300: 5.892e1

VQSLOD
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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SIO_000300: -1.783e0

MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -7.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

European (Finnish)
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: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 1.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.008767e6

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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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 3.132e0

DP
type: SiteQuality
SIO_000300: 2.008957e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.542e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
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Other
type: Population
allele count: 0
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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MQ
type: SiteQuality
SIO_000300: 5.953e1

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

South Asian
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allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

Other
type: Population
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Latino
type: Population
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allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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FS
type: SiteQuality
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.956e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

Other
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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: 11564
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.900232018561485e-4
allele num: 10344
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
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InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: -1.65e-1

ClippingRankSum
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SIO_000300: -6.54e-1

MQ
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VQSLOD
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SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

QD
type: SiteQuality
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FS
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SIO_000300: 1.05e0

MQRankSum
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SIO_000300: -3.6e-2

MQ
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -1.777e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.998980173370527e-5
allele num: 66678
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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MQRankSum
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SIO_000300: 3.6e-1

ClippingRankSum
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 19

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

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

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 17
allele frequency: 2.549643049973004e-4
allele num: 66676
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

InbreedingCoeff
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DP
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SIO_000300: 2.010492e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
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SIO_000300: 5.953e1

ClippingRankSum
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SIO_000300: -6.57e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

BaseQRankSum
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SIO_000300: 1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
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SIO_000300: 1.09e1

FS
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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FS
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VQSLOD
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.685e0

MQRankSum
type: SiteQuality
SIO_000300: -5.18e-1

DP
type: SiteQuality
SIO_000300: 2.007264e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.452e0

VQSLOD
type: SiteQuality
SIO_000300: -2.237e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.477e1

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
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: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.704e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -1.425e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.441e0

MQ
type: SiteQuality
SIO_000300: 5.807e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.647e0

DP
type: SiteQuality
SIO_000300: 2.003788e6

QD
type: SiteQuality
SIO_000300: 1.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 75
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.805e1

DP
type: SiteQuality
SIO_000300: 2.003049e6

FS
type: SiteQuality
SIO_000300: 1.432e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.955e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

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

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5103
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GenotypeQuality
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GenotypeQuality
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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: 13568
bin: 9.75e1
variant carriers: 6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.635482307319437e-4
allele num: 16504
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.282e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.377e0

DP
type: SiteQuality
SIO_000300: 1.999849e6

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-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: 3456
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.466204506065858e-4
allele num: 11540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.189e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 6.44e-1

DP
type: SiteQuality
SIO_000300: 1.997218e6

MQRankSum
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 72

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 17574

GenotypeQuality
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bin: 8.25e1
variant carriers: 50

GenotypeQuality
all individuals: 1473
bin: 8.75e1
variant carriers: 40

European (Finnish)
type: Population
allele count: 827
allele frequency: 1.253030303030303e-1
allele num: 6600
num of homozygotes: 44

Other
type: Population
allele count: 149
allele frequency: 1.655555555555556e-1
allele num: 900
num of homozygotes: 9

East Asian
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allele count: 1675
allele frequency: 1.944960520204366e-1
allele num: 8612
num of homozygotes: 168

African
type: Population
allele count: 1974
allele frequency: 1.914645974781765e-1
allele num: 10310
num of homozygotes: 193

Latino
type: Population
allele count: 1368
allele frequency: 1.188118811881188e-1
allele num: 11514
num of homozygotes: 81

European (Non-Finnish)
type: Population
allele count: 10110
allele frequency: 1.521032677378588e-1
allele num: 66468
num of homozygotes: 784

South Asian
type: Population
allele count: 3541
allele frequency: 2.146841275615375e-1
allele num: 16494
num of homozygotes: 426

VQSLOD
type: SiteQuality
SIO_000300: 6.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.711e1

DP
type: SiteQuality
SIO_000300: 2.250853e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

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
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GenotypeQuality
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GenotypeQuality
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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: 4125
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.102e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.899e0

ClippingRankSum
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SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
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SIO_000300: -1.632e0

DP
type: SiteQuality
SIO_000300: 2.044773e6

QD
type: SiteQuality
SIO_000300: 2.424e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 5.307e0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.013772942346523e-4
allele num: 66362
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ClippingRankSum
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DP
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SIO_000300: 2.033175e6

FS
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 2.073e1

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 0.0e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

South Asian
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allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 6.118e0

BaseQRankSum
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SIO_000300: -2.58e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.48594004183128e-4
allele num: 8606
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.118e0

VQSLOD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 75
allele frequency: 7.342862737419228e-3
allele num: 10214
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.475842891901286e-4
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.52420449404313e-5
allele num: 66310
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.027113e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

MQRankSum
type: SiteQuality
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QD
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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East Asian
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allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.035e0

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

European (Non-Finnish)
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allele frequency: 1.509297271190534e-5
allele num: 66256
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Latino
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African
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South Asian
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allele frequency: 6.702412868632708e-4
allele num: 16412
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Other
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European (Finnish)
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
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DP
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MQRankSum
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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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East Asian
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num of homozygotes: 0

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

East Asian
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European (Finnish)
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Other
type: Population
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Latino
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European (Non-Finnish)
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African
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6590
num of homozygotes: 0

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

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

Other
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ReadPosRankSum
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VQSLOD
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FS
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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East Asian
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allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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African
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allele num: 10388
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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QD
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.06e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

East Asian
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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African
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -2.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

DP
type: SiteQuality
SIO_000300: 1.962639e6

QD
type: SiteQuality
SIO_000300: 9.73e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

South Asian
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allele num: 16484
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Other
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East Asian
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allele frequency: 0.0e0
allele num: 8622
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66558
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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DP
type: SiteQuality
SIO_000300: 1.962911e6

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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SIO_000300: 2.5e0

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.155e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66586
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East Asian
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Other
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South Asian
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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DP
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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DP
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VQSLOD
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FS
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ClippingRankSum
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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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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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Other
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South Asian
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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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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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.957063e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 1.162e1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 1681
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
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: 11504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

DP
type: SiteQuality
SIO_000300: 1.943542e6

QD
type: SiteQuality
SIO_000300: 7.18e0

VQSLOD
type: SiteQuality
SIO_000300: -6.524e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

GenotypeQuality
all individuals: 1917
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29863
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.917720287881735e-4
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65014
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 1.776e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

DP
type: SiteQuality
SIO_000300: 1.877276e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.471e1

GenotypeQuality
all individuals: 5876
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

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

GenotypeQuality
all individuals: 2107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6660
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3304
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553904963172452e-5
allele num: 64354
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.876e-1

DP
type: SiteQuality
SIO_000300: 1.800024e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 4.463e0

QD
type: SiteQuality
SIO_000300: 1.769e1

GenotypeQuality
all individuals: 201
bin: 2.5e0
variant carriers: 9

GenotypeQuality
all individuals: 551
bin: 5.25e1
variant carriers: 90

GenotypeQuality
all individuals: 844
bin: 8.25e1
variant carriers: 119

GenotypeQuality
all individuals: 214
bin: 7.5e0
variant carriers: 18

GenotypeQuality
all individuals: 2391
bin: 3.75e1
variant carriers: 49

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 73

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 12

GenotypeQuality
all individuals: 196
bin: 1.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1184
bin: 7.75e1
variant carriers: 156

GenotypeQuality
all individuals: 866
bin: 7.25e1
variant carriers: 63

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 87

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 108

GenotypeQuality
all individuals: 6156
bin: 2.25e1
variant carriers: 24

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 83

European (Finnish)
type: Population
allele count: 817
allele frequency: 1.260024676125848e-1
allele num: 6484
num of homozygotes: 40

East Asian
type: Population
allele count: 1614
allele frequency: 1.966374269005848e-1
allele num: 8208
num of homozygotes: 152

South Asian
type: Population
allele count: 3465
allele frequency: 2.141797502781555e-1
allele num: 16178
num of homozygotes: 407

Other
type: Population
allele count: 142
allele frequency: 1.602708803611738e-1
allele num: 886
num of homozygotes: 8

African
type: Population
allele count: 2238
allele frequency: 2.195839874411303e-1
allele num: 10192
num of homozygotes: 246

Latino
type: Population
allele count: 1328
allele frequency: 1.184656556645852e-1
allele num: 11210
num of homozygotes: 79

European (Non-Finnish)
type: Population
allele count: 9579
allele frequency: 1.504239949748744e-1
allele num: 63680
num of homozygotes: 697

DP
type: SiteQuality
SIO_000300: 1.802811e6

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

QD
type: SiteQuality
SIO_000300: 1.817e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 905
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variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5196
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 515
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variant carriers: 0

GenotypeQuality
all individuals: 3958
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variant carriers: 0

GenotypeQuality
all individuals: 3675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4932
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63050
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.958967926894822e-5
allele num: 11162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15984
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.245e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.355e1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
type: SiteQuality
SIO_000300: 1.595297e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

GenotypeQuality
all individuals: 416
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8698
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6471
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2490
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2556
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15858
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.60627088152146e-5
allele num: 62256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.54447e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5210
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 509
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 630
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7697
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 19
allele frequency: 1.203445654927793e-3
allele num: 15788
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

DP
type: SiteQuality
SIO_000300: 1.52342e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

QD
type: SiteQuality
SIO_000300: 1.636e1

GenotypeQuality
all individuals: 2569
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4906
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3866
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5105
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3178
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23721
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.187366421277606e-4
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.57832e6

VQSLOD
type: SiteQuality
SIO_000300: -3.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1254
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 2.75e1
variant carriers: 0

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

Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 15824
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64890
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East Asian
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allele frequency: 1.173708920187793e-4
allele num: 8520
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -4.0e-4

FS
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ReadPosRankSum
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MQ
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SIO_000300: 5.956e1

MQRankSum
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SIO_000300: 3.54e-1

QD
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SIO_000300: 1.184e1

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.694529e6

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

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

Latino
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allele frequency: 8.926977325477593e-5
allele num: 11202
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8536
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 4.0e-4

VQSLOD
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DP
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ClippingRankSum
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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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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.528771479239283e-5
allele num: 65412
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6462
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Other
type: Population
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

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

DP
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FS
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

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

South Asian
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allele count: 1
allele frequency: 6.268020559107433e-5
allele num: 15954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65466
num of homozygotes: 0

Other
type: Population
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MQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.105e0

InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.057e0

FS
type: SiteQuality
SIO_000300: 6.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.86e-1

DP
type: SiteQuality
SIO_000300: 1.732405e6

MQ
type: SiteQuality
SIO_000300: 5.826e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.07e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6472
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.525785779676533e-5
allele num: 65540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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Other
type: Population
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

MQ
type: SiteQuality
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 7.563e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.526624328285296e-5
allele num: 65504
num of homozygotes: 0

South Asian
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African
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allele frequency: 0.0e0
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Latino
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East Asian
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Other
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European (Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Latino
type: Population
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Other
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65190
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East Asian
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South Asian
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MQ
type: SiteQuality
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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African
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allele num: 9776
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Latino
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Other
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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SIO_000300: 7.72e0

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

DP
type: SiteQuality
SIO_000300: 1.693575e6

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578332649389185e-5
allele num: 63358
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

FS
type: SiteQuality
SIO_000300: 7.72e0

ReadPosRankSum
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SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.693575e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.052e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.011e0

QD
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SIO_000300: 8.800000000000001e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10926
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.029018316526034e-4
allele num: 9718
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.676334e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 1.615e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.42e0

QD
type: SiteQuality
SIO_000300: 1.412e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.282051282051282e-4
allele num: 7800
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.68e-1

FS
type: SiteQuality
SIO_000300: 1.351e0

QD
type: SiteQuality
SIO_000300: 7.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.519217e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.096972356296621e-4
allele num: 9116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.24e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.21e-1

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.468212e6

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.474e0

FS
type: SiteQuality
SIO_000300: 2.678e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14406
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.275652862041678e-4
allele num: 7582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.444295e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.56e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 780
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.772169844757922e-5
allele num: 56428
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

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